FDA 510(k)

CLARICEL STERILIZATION POUCHES AND STERILIZATION REELS

K-Number: K972719 · 1999-02-04

Decision Date1999-02-04

Product CodeKCT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

CLARICEL STERILIZATION POUCHES AND STERILIZATION REELS is the device name listed in this FDA 510(k) record. The listed applicant is Medicel, S.A. DE C.V.. It received FDA 510(k) clearance on 1999-02-04 under 510(k) number K972719. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLARICEL STERILIZATION POUCHES AND STERILIZATION REELS?

CLARICEL STERILIZATION POUCHES AND STERILIZATION REELS is a medical device that received FDA 510(k) clearance on 1999-02-04. The listed applicant is Medicel, S.A. DE C.V.. The 510(k) number is K972719.

When did CLARICEL STERILIZATION POUCHES AND STERILIZATION REELS receive FDA 510(k) clearance?

CLARICEL STERILIZATION POUCHES AND STERILIZATION REELS received FDA 510(k) clearance on 1999-02-04, under 510(k) number K972719.

Who is the listed applicant for CLARICEL STERILIZATION POUCHES AND STERILIZATION REELS?

The FDA 510(k) record lists Medicel, S.A. DE C.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLARICEL STERILIZATION POUCHES AND STERILIZATION REELS?

The FDA product code for CLARICEL STERILIZATION POUCHES AND STERILIZATION REELS is KCT.

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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.