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FDA 510(k)

HISTOCAN BIOPSY NEEDLE

K-Number: K813081 · 1981-12-29

ApplicantBurron Medical Products, Inc.
Decision Date1981-12-29
Product Code
DecisionSubstantially Equivalent

Device Summary

HISTOCAN BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical Products, Inc.. It received FDA 510(k) clearance on 1981-12-29 under 510(k) number K813081. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HISTOCAN BIOPSY NEEDLE?

HISTOCAN BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1981-12-29. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K813081.

When did HISTOCAN BIOPSY NEEDLE receive FDA 510(k) clearance?

HISTOCAN BIOPSY NEEDLE received FDA 510(k) clearance on 1981-12-29, under 510(k) number K813081.

Who is the listed applicant for HISTOCAN BIOPSY NEEDLE?

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

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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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