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FDA 510(k)

ADAPTER BE 105-101 & 125-101

K-Number: K770634 · 1977-04-08

ApplicantInstrumentation Industries, Inc.
Decision Date1977-04-08
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ADAPTER BE 105-101 & 125-101 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 1977-04-08 under 510(k) number K770634. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAPTER BE 105-101 & 125-101?

ADAPTER BE 105-101 & 125-101 is a medical device that received FDA 510(k) clearance on 1977-04-08. The listed applicant is Instrumentation Industries, Inc.. The 510(k) number is K770634.

When did ADAPTER BE 105-101 & 125-101 receive FDA 510(k) clearance?

ADAPTER BE 105-101 & 125-101 received FDA 510(k) clearance on 1977-04-08, under 510(k) number K770634.

Who is the listed applicant for ADAPTER BE 105-101 & 125-101?

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 BE 105-101 & 125-101?

The FDA product code for ADAPTER BE 105-101 & 125-101 is BZA.

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Related Devices (Code: BZA)

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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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