FDA 510(k)

BERAHA BIOPSY NEEDLES, 2N2730, 2N2731 & 2N2732

K-Number: K855003 · 1986-02-10

Decision Date1986-02-10

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BERAHA BIOPSY NEEDLES, 2N2730, 2N2731 & 2N2732 is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1986-02-10 under 510(k) number K855003. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BERAHA BIOPSY NEEDLES, 2N2730, 2N2731 & 2N2732?

BERAHA BIOPSY NEEDLES, 2N2730, 2N2731 & 2N2732 is a medical device that received FDA 510(k) clearance on 1986-02-10. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K855003.

When did BERAHA BIOPSY NEEDLES, 2N2730, 2N2731 & 2N2732 receive FDA 510(k) clearance?

BERAHA BIOPSY NEEDLES, 2N2730, 2N2731 & 2N2732 received FDA 510(k) clearance on 1986-02-10, under 510(k) number K855003.

Who is the listed applicant for BERAHA BIOPSY NEEDLES, 2N2730, 2N2731 & 2N2732?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BERAHA BIOPSY NEEDLES, 2N2730, 2N2731 & 2N2732?

The FDA product code for BERAHA BIOPSY NEEDLES, 2N2730, 2N2731 & 2N2732 is KNW.

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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.