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FDA 510(k)

UNINHIBITED

K-Number: K021503 · 2002-08-01

ApplicantBisco, Inc.
Decision Date2002-08-01
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UNINHIBITED is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 2002-08-01 under 510(k) number K021503. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNINHIBITED?

UNINHIBITED is a medical device that received FDA 510(k) clearance on 2002-08-01. The listed applicant is Bisco, Inc.. The 510(k) number is K021503.

When did UNINHIBITED receive FDA 510(k) clearance?

UNINHIBITED received FDA 510(k) clearance on 2002-08-01, under 510(k) number K021503.

Who is the listed applicant for UNINHIBITED?

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

What is the FDA product code for UNINHIBITED?

The FDA product code for UNINHIBITED is EBD.

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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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