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FDA 510(k)

K-BAND AND K-CREPE

K-Number: K926072 · 1993-03-19

ApplicantParema , Ltd.
Decision Date1993-03-19
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

K-BAND AND K-CREPE is the device name listed in this FDA 510(k) record. The listed applicant is Parema , Ltd.. It received FDA 510(k) clearance on 1993-03-19 under 510(k) number K926072. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-BAND AND K-CREPE?

K-BAND AND K-CREPE is a medical device that received FDA 510(k) clearance on 1993-03-19. The listed applicant is Parema , Ltd.. The 510(k) number is K926072.

When did K-BAND AND K-CREPE receive FDA 510(k) clearance?

K-BAND AND K-CREPE received FDA 510(k) clearance on 1993-03-19, under 510(k) number K926072.

Who is the listed applicant for K-BAND AND K-CREPE?

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

What is the FDA product code for K-BAND AND K-CREPE?

The FDA product code for K-BAND AND K-CREPE is NAB.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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