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FDA 510(k)

REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS

K-Number: K033578 · 2005-07-11

ApplicantClearmedical, Inc.
Decision Date2005-07-11
Product CodeNLL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS is the device name listed in this FDA 510(k) record. The listed applicant is Clearmedical, Inc.. It received FDA 510(k) clearance on 2005-07-11 under 510(k) number K033578. The device is classified under product code NLL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS?

REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS is a medical device that received FDA 510(k) clearance on 2005-07-11. The listed applicant is Clearmedical, Inc.. The 510(k) number is K033578.

When did REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS receive FDA 510(k) clearance?

REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS received FDA 510(k) clearance on 2005-07-11, under 510(k) number K033578.

Who is the listed applicant for REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS?

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 RELOADABLE CUTTERS, STAPLERS, AND APPLIERS?

The FDA product code for REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS is NLL.

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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.

K033579REPROCESSED MULTIPLE CLIP APPLIERSK033591REPROCESSED TROCARSK033592REPROCESSED SURGICAL SCISSORS AND GRASPERSK033593REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPSK031416CLEARMEDICAL/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: NLL)

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.

K070930REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERSSterilmed, Inc.K070859REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERSSterilmed, 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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