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FDA 510(k)

BARNARD & ASSOCIATES REMANUFACTURED GENERAL PURPOSE, VACUUM OR LABORATORY STERILIZER

K-Number: K950341 · 1995-04-19

ApplicantBarnard and Assoc.
Decision Date1995-04-19
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BARNARD & ASSOCIATES REMANUFACTURED GENERAL PURPOSE, VACUUM OR LABORATORY STERILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Barnard and Assoc.. It received FDA 510(k) clearance on 1995-04-19 under 510(k) number K950341. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARNARD & ASSOCIATES REMANUFACTURED GENERAL PURPOSE, VACUUM OR LABORATORY STERILIZER?

BARNARD & ASSOCIATES REMANUFACTURED GENERAL PURPOSE, VACUUM OR LABORATORY STERILIZER is a medical device that received FDA 510(k) clearance on 1995-04-19. The listed applicant is Barnard and Assoc.. The 510(k) number is K950341.

When did BARNARD & ASSOCIATES REMANUFACTURED GENERAL PURPOSE, VACUUM OR LABORATORY STERILIZER receive FDA 510(k) clearance?

BARNARD & ASSOCIATES REMANUFACTURED GENERAL PURPOSE, VACUUM OR LABORATORY STERILIZER received FDA 510(k) clearance on 1995-04-19, under 510(k) number K950341.

Who is the listed applicant for BARNARD & ASSOCIATES REMANUFACTURED GENERAL PURPOSE, VACUUM OR LABORATORY STERILIZER?

The FDA 510(k) record lists Barnard and Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARNARD & ASSOCIATES REMANUFACTURED GENERAL PURPOSE, VACUUM OR LABORATORY STERILIZER?

The FDA product code for BARNARD & ASSOCIATES REMANUFACTURED GENERAL PURPOSE, VACUUM OR LABORATORY STERILIZER is FLE.

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Related Devices (Code: FLE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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