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FDA 510(k)

FLEX ARM BE 122, CLAMP 122-27

K-Number: K770631 · 1977-05-23

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

Device Summary

FLEX ARM BE 122, CLAMP 122-27 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 K770631. The device is classified under product code JAY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEX ARM BE 122, CLAMP 122-27?

FLEX ARM BE 122, CLAMP 122-27 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 K770631.

When did FLEX ARM BE 122, CLAMP 122-27 receive FDA 510(k) clearance?

FLEX ARM BE 122, CLAMP 122-27 received FDA 510(k) clearance on 1977-05-23, under 510(k) number K770631.

Who is the listed applicant for FLEX ARM BE 122, CLAMP 122-27?

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 FLEX ARM BE 122, CLAMP 122-27?

The FDA product code for FLEX ARM BE 122, CLAMP 122-27 is JAY.

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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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