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FDA 510(k)

ADAPTER, VALVE, ONE WAY BE-130-22

K-Number: K770627 · 1977-05-23

ApplicantInstrumentation Industries, Inc.
Decision Date1977-05-23
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ADAPTER, VALVE, ONE WAY BE-130-22 is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Industries, Inc.. It received FDA 510(k) clearance on 1977-05-23 under 510(k) number K770627. The device is classified under product code CBP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAPTER, VALVE, ONE WAY BE-130-22?

ADAPTER, VALVE, ONE WAY BE-130-22 is a medical device that received FDA 510(k) clearance on 1977-05-23. The listed applicant is Instrumentation Industries, Inc.. The 510(k) number is K770627.

When did ADAPTER, VALVE, ONE WAY BE-130-22 receive FDA 510(k) clearance?

ADAPTER, VALVE, ONE WAY BE-130-22 received FDA 510(k) clearance on 1977-05-23, under 510(k) number K770627.

Who is the listed applicant for ADAPTER, VALVE, ONE WAY BE-130-22?

The FDA 510(k) record lists Instrumentation Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADAPTER, VALVE, ONE WAY BE-130-22?

The FDA product code for ADAPTER, VALVE, ONE WAY BE-130-22 is CBP.

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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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