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FDA 510(k)

BURRON MICROCATH INTRA. CATH. PLACEMENTT

K-Number: K801941 · 1980-08-27

ApplicantBurron Medical Products, Inc.
Decision Date1980-08-27
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BURRON MICROCATH INTRA. CATH. PLACEMENTT 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 1980-08-27 under 510(k) number K801941. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BURRON MICROCATH INTRA. CATH. PLACEMENTT?

BURRON MICROCATH INTRA. CATH. PLACEMENTT is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K801941.

When did BURRON MICROCATH INTRA. CATH. PLACEMENTT receive FDA 510(k) clearance?

BURRON MICROCATH INTRA. CATH. PLACEMENTT received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801941.

Who is the listed applicant for BURRON MICROCATH INTRA. CATH. PLACEMENTT?

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

What is the FDA product code for BURRON MICROCATH INTRA. CATH. PLACEMENTT?

The FDA product code for BURRON MICROCATH INTRA. CATH. PLACEMENTT is FOZ.

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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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