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FDA 510(k)

VALVE, PRESSURE, DEMAND

K-Number: K770665 · 1977-04-15

ApplicantMcgaw Respiratory Therapy
Decision Date1977-04-15
Product CodeCBD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VALVE, PRESSURE, DEMAND is the device name listed in this FDA 510(k) record. The listed applicant is Mcgaw Respiratory Therapy. It received FDA 510(k) clearance on 1977-04-15 under 510(k) number K770665. The device is classified under product code CBD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALVE, PRESSURE, DEMAND?

VALVE, PRESSURE, DEMAND is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is Mcgaw Respiratory Therapy. The 510(k) number is K770665.

When did VALVE, PRESSURE, DEMAND receive FDA 510(k) clearance?

VALVE, PRESSURE, DEMAND received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770665.

Who is the listed applicant for VALVE, PRESSURE, DEMAND?

The FDA 510(k) record lists Mcgaw Respiratory Therapy as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VALVE, PRESSURE, DEMAND?

The FDA product code for VALVE, PRESSURE, DEMAND is CBD.

Related Clinical Trials

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Other records listing Mcgaw Respiratory Therapy as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K771550MRT DISPENSORK771516CAPILLARY SAMPLE LINEK770286VENTILATOR BREATHING CIRCUITK761299DISPOSABLE NEBULIZERK761300NEBULIZER CONTROL UNITK761298PRE-FILLED DISPOSABLE NEBULIZER

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Related Devices (Code: CBD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K780340IMV SYSTEMLkb Instruments, Inc.K770369VACON TMDiemolding Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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