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FDA 510(k)

BIOTROL BUN ENZYMATIQUE UV H.P.

K-Number: K881366 · 1988-05-16

ApplicantBiotrol, USA, Inc.
Decision Date1988-05-16
Product CodeCDQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BIOTROL BUN ENZYMATIQUE UV H.P. is the device name listed in this FDA 510(k) record. The listed applicant is Biotrol, USA, Inc.. It received FDA 510(k) clearance on 1988-05-16 under 510(k) number K881366. The device is classified under product code CDQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOTROL BUN ENZYMATIQUE UV H.P.?

BIOTROL BUN ENZYMATIQUE UV H.P. is a medical device that received FDA 510(k) clearance on 1988-05-16. The listed applicant is Biotrol, USA, Inc.. The 510(k) number is K881366.

When did BIOTROL BUN ENZYMATIQUE UV H.P. receive FDA 510(k) clearance?

BIOTROL BUN ENZYMATIQUE UV H.P. received FDA 510(k) clearance on 1988-05-16, under 510(k) number K881366.

Who is the listed applicant for BIOTROL BUN ENZYMATIQUE UV H.P.?

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

What is the FDA product code for BIOTROL BUN ENZYMATIQUE UV H.P.?

The FDA product code for BIOTROL BUN ENZYMATIQUE UV H.P. is CDQ.

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Related Devices (Code: CDQ)

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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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