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FDA 510(k)

BRACKET BE 122-1

K-Number: K770633 · 1977-05-23

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

Device Summary

BRACKET BE 122-1 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 K770633. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRACKET BE 122-1?

BRACKET BE 122-1 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 K770633.

When did BRACKET BE 122-1 receive FDA 510(k) clearance?

BRACKET BE 122-1 received FDA 510(k) clearance on 1977-05-23, under 510(k) number K770633.

Who is the listed applicant for BRACKET BE 122-1?

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 BRACKET BE 122-1?

The FDA product code for BRACKET BE 122-1 is CAF.

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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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