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FDA 510(k)

LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER

K-Number: K812744 · 1981-12-03

ApplicantProgress Mankind Technology
Decision Date1981-12-03
Product CodeHAW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Progress Mankind Technology. It received FDA 510(k) clearance on 1981-12-03 under 510(k) number K812744. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER?

LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER is a medical device that received FDA 510(k) clearance on 1981-12-03. The listed applicant is Progress Mankind Technology. The 510(k) number is K812744.

When did LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER receive FDA 510(k) clearance?

LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER received FDA 510(k) clearance on 1981-12-03, under 510(k) number K812744.

Who is the listed applicant for LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER?

The FDA 510(k) record lists Progress Mankind Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER?

The FDA product code for LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER is HAW.

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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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