Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K094003
    Device Name
    REVIVATOR
    Manufacturer
    Date Cleared
    2010-09-17

    (263 days)

    Product Code
    Regulation Number
    868.5915
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Revivator resuscitator is intended for pulmonary resuscitation.
    The adult resuscitator is for people with a body weight of more than 30 kg (66 lbs)
    The child resuscitator is for children with a body weight between 7 and 30 kg (15-66 lbs)
    The infant resuscitator is for infants with a body weight up to 7 kg (15 lbs)

    Device Description

    A resuscitator is a device using positive pressure to inflate the lungs of an unconscious person who is not breathing, in order to keep him oxygenated and alive. The manual resuscitators basically consist of a mask and a large hand-squeezed plastic bulb using ambient air, or supplemental oxygen. The air and oxygen flows into the resuscitator bag. And compressing the bag, the patient is ventilated. In order not to apply a high pressure to the patient's airways, the resuscitators include a pressure-limiting valve.

    AI/ML Overview

    1. Acceptance Criteria and Reported Device Performance

    The device, "Revivator" manual resuscitator, claims substantial equivalence to predicate devices based on compliance with the ISO 10651-4:2002 standard for lung ventilators. The acceptance criteria are derived from this standard. The reported device performance is compared against these criteria and the performance of predicate devices.

    Acceptance Criteria (ISO 10651-4:2002)Revivator Performance (Adult, Child, Infant)Predicate Device Performance (Ambu & Mercury Medical Resuscitators)
    Pressure-limiting valve for 10 kg body weight: Not higher than 6 kPa (60 cm H2O) (if included, optional)Adult: 6 kPa (60 cm H2O)Adult: 4.0 kPa (Ambu Spur II); Optional for small adults (Mercury Med)
    Max. tidal volume for 40 kg body weight: At least 600 mLAdult: 1000 mLMeets standard
    Delivered oxygen concentration (with O2 source) : At least 85% (V/V) (with attachment)Without reservoir: 39-88% O2 (at 2-15 L/min O2 flow); With reservoir: 98-100% O2 (at 2-15 L/min O2 flow)Claimed to meet standard (reservoir volume contributes)
    Apparatus dead space: Shall not exceed 5 mL + 10 % of the minimum delivered volumeLower than 7 mLBetween 5 and 7 mL
    Expiratory resistance: Shall not exceed 5 cm H2O0.09 cm H2O (at 5 L/min); 1.76 cm H2O (at 50 L/min)Values much lower than admissible
    Inspiratory resistance: Shall not exceed 5 cm H2O below atmospheric pressure0.37 cm H2O (at 5 L/min); 3.48 cm H2O (at 50 L/min)Values much lower than admissible (Ambu Spur II adult/pediatric 5 cm H2O at 50 L/min)
    Patient connectors: 22/15 mm22mm male / 15mm femaleIn conformity (Ambu)
    Expiratory connectors: 30 mm male30mm male (PEEP/AGSS)In conformity (Ambu)
    Bag refill valve connectors: 32 mm female conical32 mm femaleIn conformity (Predicate devices)
    Storage temperatures: -40°C to +60°C (with 40%-95% r.h.)-40°C to +70°CAll resuscitators meet; Revivator & Ambu reusable can store at 70°C
    Operating temperatures: -18°C to +50°C (with 40%-95% r.h.)-20°C to +60°CAll resuscitators meet; Revivator & Ambu reusable can operate at -20°C
    Dismantling & reassembly: Functional test after reassemblyIncludes functional test in labelingIncludes functional test in labeling
    Patient Valve function after contamination with vomitus: In conformity with standardIn conformity with standardIn conformity with standard
    Drop test: In conformity with standardIn conformity with standardIn conformity with standard
    Immersion in water: In conformity with standardIn conformity with standardIn conformity with standard
    End-expiratory pressure: If > 0.2 kPa, value in instructions; pressure gradient
    Ask a Question

    Ask a specific question about this device

    Page 1 of 1