FDA 510(k)

REPROCESSED SURGICAL SCISSORS AND GRASPERS

K-Number: K033592 · 2004-07-27

Decision Date2004-07-27

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

REPROCESSED SURGICAL SCISSORS AND GRASPERS is the device name listed in this FDA 510(k) record. The listed applicant is Clearmedical, Inc.. It received FDA 510(k) clearance on 2004-07-27 under 510(k) number K033592. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED SURGICAL SCISSORS AND GRASPERS?

REPROCESSED SURGICAL SCISSORS AND GRASPERS is a medical device that received FDA 510(k) clearance on 2004-07-27. The listed applicant is Clearmedical, Inc.. The 510(k) number is K033592.

When did REPROCESSED SURGICAL SCISSORS AND GRASPERS receive FDA 510(k) clearance?

REPROCESSED SURGICAL SCISSORS AND GRASPERS received FDA 510(k) clearance on 2004-07-27, under 510(k) number K033592.

Who is the listed applicant for REPROCESSED SURGICAL SCISSORS AND GRASPERS?

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

What is the FDA product code for REPROCESSED SURGICAL SCISSORS AND GRASPERS?

The FDA product code for REPROCESSED SURGICAL SCISSORS AND GRASPERS is GEI.

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Other records listing Clearmedical, Inc. as applicant

K033579REPROCESSED MULTIPLE CLIP APPLIERS K033578REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS K033591REPROCESSED TROCARS K033593REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS K031416CLEARMEDICAL/CRITIKON BLOOD PRESSURE CUFF; CLEARMEDICAL/WELCH ALLYN BLOOD PRESSURE CUFF K012600CLEARMEDICAL/NELLCOR OXISENSOR II, ADULT, MODEL D-25/D-25L

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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.