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FDA 510(k)

MINISAMPLER TM

K-Number: K822508 · 1982-10-22

ApplicantBms, Inc.
Decision Date1982-10-22
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MINISAMPLER TM is the device name listed in this FDA 510(k) record. The listed applicant is Bms, Inc.. It received FDA 510(k) clearance on 1982-10-22 under 510(k) number K822508. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINISAMPLER TM?

MINISAMPLER TM is a medical device that received FDA 510(k) clearance on 1982-10-22. The listed applicant is Bms, Inc.. The 510(k) number is K822508.

When did MINISAMPLER TM receive FDA 510(k) clearance?

MINISAMPLER TM received FDA 510(k) clearance on 1982-10-22, under 510(k) number K822508.

Who is the listed applicant for MINISAMPLER TM?

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

What is the FDA product code for MINISAMPLER TM?

The FDA product code for MINISAMPLER TM is JKA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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