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510(k) Data Aggregation
(39 days)
Used as an indoor and outdoor mobility assistive device. Never used as a transportation tool on highways and freeways.
The Jupiter 50 electric scooter is a mobility assistive device for physically challenged people and elderly people. It is motorized by a 24V DC motor. Two or four 12 volt batteries supply electrical power. Jupiter 50 consists of seven major components: chassis, body covers, transaxle, seat, controller, batteries, and battery charger.
The provided text describes a 510(k) summary for the Jupiter 50 Scooter, a mobility assistive device. It focuses on demonstrating substantial equivalence to a predicate device (Pride Health Care Legend Scooter) rather than establishing novel acceptance criteria or conducting studies as would be performed for a new, high-risk medical device.
Therefore, many of the requested elements for describing "acceptance criteria and the study that proves the device meets the acceptance criteria" are not applicable or explicitly stated in this type of submission. The information provided is primarily for regulatory clearance based on substantial equivalence.
Here's the breakdown of what can be extracted and what cannot:
1. A table of acceptance criteria and the reported device performance
The submission does not define "acceptance criteria" in the typical sense of a clinical or performance study with pre-specified thresholds. Instead, it presents a comparison of the Jupiter 50's features and performance against a predicate device (Legend SC 300) to demonstrate substantial equivalence. The "performance" is reported by comparing specifications.
Characteristic | Acceptance Criteria (Implied by Predicate) | Reported Device Performance (Jupiter 50) |
---|---|---|
Number of wheels | 3 (for Legend SC 300, though listed as 1/3) | 3 |
Wheel size | 2 Rear 10", Front 9" | 3 x 10" |
Width | 24" | 600 mm (24") |
Length | 47" | 1200 mm (47.2") |
Ground Clearance | 4.25" | 100 mm (4") |
Weight w/o batteries | 105 lb. | 107 lb. |
Seat style | fish-on | fish-on |
Speed | 0 - 5.25 mph | 0 - 8.0 km/h (0 -5.0 miles/h) |
Number of Batteries | 2 | 2 or 4 |
Travel Range | 25 miles | 40 km (25 miles) or 75 km (47 miles) |
Motor Size, Cont. hp. | 0.6 hp | 400 W (0.55 hp) |
Maximum battery size | 2 x 12V-30Ah | 4 x 12V-30Ah |
Grade climbable | 15 degrees | 12 degrees |
Carrying Capacity | 250 lb. | 250 lb. |
Number of disassembly parts | 5 | 5 |
Weight of heaviest part | 49 lb. | 55 lb. |
Auxiliary Safety Casters | None | 2 |
Dynamic Electric Brake | Yes | Yes |
Turning lights | Optional | Yes |
Head Light | Optional | Yes |
The device was also tested against and passed several ISO 7176 standards (1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 14, and 16) and British Standard BS5852 (equivalent to California Bulletin 116 and 117 for fire retardantness). These standards represent performance and safety criteria, and passing them serves as evidence of meeting acceptance criteria for specific technical aspects.
2. Sample size used for the test set and the data provenance (e.g. country of origin of the data, retrospective or prospective)
This information is not provided in the document. The submission references "The testing and comparative study" but does not detail the methodology, sample sizes, or data provenance for these studies beyond stating the device has been sold in China for over a year "with no safety problems".
3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts (e.g. radiologist with 10 years of experience)
This information is not applicable as this is a mechanical device, not an AI or diagnostic device requiring expert interpretation for ground truth.
4. Adjudication method (e.g. 2+1, 3+1, none) for the test set
This information is not applicable as this is a mechanical device, not an AI or diagnostic device requiring expert interpretation for ground truth.
5. If a multi reader multi case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance
This information is not applicable. This is not an AI-based diagnostic device.
6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done
This information is not applicable. This is not an AI-based device.
7. The type of ground truth used (expert consensus, pathology, outcomes data, etc)
For the technical specifications, the "ground truth" is measured physical and performance characteristics against established engineering specifications and predicate device performance. For safety and standards compliance, the ground truth is adherence to the requirements of the specified ISO standards and fire retardantness standards. The claim of "no safety problems" in China over a year could be considered a form of real-world outcomes data, though not a formal "ground truth" for a specific test set.
8. The sample size for the training set
This information is not applicable. This is not an AI-based device that requires a training set.
9. How the ground truth for the training set was established
This information is not applicable. This is not an AI-based device that requires a training set.
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