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FDA 510(k)

THE RED CAP

K-Number: K820454 · 1982-03-08

ApplicantBurron Medical Products, Inc.
Decision Date1982-03-08
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THE RED CAP 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 1982-03-08 under 510(k) number K820454. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE RED CAP?

THE RED CAP is a medical device that received FDA 510(k) clearance on 1982-03-08. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K820454.

When did THE RED CAP receive FDA 510(k) clearance?

THE RED CAP received FDA 510(k) clearance on 1982-03-08, under 510(k) number K820454.

Who is the listed applicant for THE RED CAP?

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 THE RED CAP?

The FDA product code for THE RED CAP is FMF.

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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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