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FDA 510(k)

REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS

K-Number: K033593 · 2003-11-20

ApplicantClearmedical, Inc.
Decision Date2003-11-20
Product CodeNLU
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Clearmedical, Inc.. It received FDA 510(k) clearance on 2003-11-20 under 510(k) number K033593. The device is classified under product code NLU. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS?

REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 2003-11-20. The listed applicant is Clearmedical, Inc.. The 510(k) number is K033593.

When did REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS receive FDA 510(k) clearance?

REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS received FDA 510(k) clearance on 2003-11-20, under 510(k) number K033593.

Who is the listed applicant for REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS?

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 SINGLE USE DEVICES BIOPSY FORCEPS?

The FDA product code for REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS is NLU.

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Other records listing Clearmedical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K033578REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERSK033579REPROCESSED MULTIPLE CLIP APPLIERSK033591REPROCESSED TROCARSK033592REPROCESSED SURGICAL SCISSORS AND GRASPERSK031416CLEARMEDICAL/CRITIKON BLOOD PRESSURE CUFF; CLEARMEDICAL/WELCH ALLYN BLOOD PRESSURE CUFFK012600CLEARMEDICAL/NELLCOR OXISENSOR II, ADULT, MODEL D-25/D-25L

View all 14 devices →

Related Devices (Code: NLU)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K050136REPROCESSED HOT BIOPSY FORCEPSSterilmed, Inc.K024011SISS REPROCESSED HOT BIOPSY FORCEPS, LAPAROSCOPIC, ENDOSCOPIC AND ELECTROSURGICAL SURGICAL INSTRUMENTS AND ACCESSORIESSurgical Instruments Service and Savings, Inc.K011800VANGUARD REPROCESSED ELECTRIC BIOPSY FORCEPSVanguard Medical Concepts, Inc.

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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