K Number
K983227
Device Name
POWER BLOCK
Manufacturer
Date Cleared
1998-12-11

(87 days)

Product Code
Regulation Number
872.6300
Panel
DE
Reference & Predicate Devices
N/A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use

PowerBlock is a white, light reflective, paint on dam which, when light cured, will form a semi-plastic barrier which protects gingival tissue.

Device Description

PowerBlock is a white, light reflective, paint on dam.

AI/ML Overview

This is a 510(k) clearance letter for the PowerBlock device. It indicates that the device has been found substantially equivalent to a predicate device. However, it does not contain the detailed study information required to answer your specific questions about acceptance criteria and device performance studies.

Therefore, I cannot provide the information requested in your prompt based on the provided text. To answer your questions, I would need a different document, such as a summary of safety and effectiveness, or the full 510(k) submission which would include the performance data.

§ 872.6300 Rubber dam and accessories.

(a)
Identification. A rubber dam and accessories is a device composed of a thin sheet of latex with a hole in the center intended to isolate a tooth from fluids in the mouth during dental procedures, such as filling a cavity preparation. The device is stretched around a tooth by inserting a tooth through a hole in the center. The device includes the rubber dam, rubber dam clamp, rubber dam frame, and forceps for a rubber dam clamp. This classification does not include devices intended for use in preventing transmission of sexually transmitted diseases through oral sex; those devices are classified as condoms in § 884.5300 of this chapter.(b)
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 872.9. If the device is not labeled or otherwise represented as sterile, it is exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of § 820.180 of this chapter, with respect to general requirements concerning records, and § 820.198 of this chapter, with respect to complaint files.