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FDA 510(k)

BE#6006 VAR. RESIS. INSPIR. MUSCLE

K-Number: K821492 · 1982-09-24

ApplicantInstrumentation Industries, Inc.
Decision Date1982-09-24
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BE#6006 VAR. RESIS. INSPIR. MUSCLE 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 1982-09-24 under 510(k) number K821492. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BE#6006 VAR. RESIS. INSPIR. MUSCLE?

BE#6006 VAR. RESIS. INSPIR. MUSCLE is a medical device that received FDA 510(k) clearance on 1982-09-24. The listed applicant is Instrumentation Industries, Inc.. The 510(k) number is K821492.

When did BE#6006 VAR. RESIS. INSPIR. MUSCLE receive FDA 510(k) clearance?

BE#6006 VAR. RESIS. INSPIR. MUSCLE received FDA 510(k) clearance on 1982-09-24, under 510(k) number K821492.

Who is the listed applicant for BE#6006 VAR. RESIS. INSPIR. MUSCLE?

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 BE#6006 VAR. RESIS. INSPIR. MUSCLE?

The FDA product code for BE#6006 VAR. RESIS. INSPIR. MUSCLE is BWF.

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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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