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FDA 510(k)

SUTURE REMOVAL KIT

K-Number: K941465 · 1994-04-22

ApplicantClinical Resources, Inc.
Decision Date1994-04-22
Product CodeMCZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUTURE REMOVAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Resources, Inc.. It received FDA 510(k) clearance on 1994-04-22 under 510(k) number K941465. The device is classified under product code MCZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTURE REMOVAL KIT?

SUTURE REMOVAL KIT is a medical device that received FDA 510(k) clearance on 1994-04-22. The listed applicant is Clinical Resources, Inc.. The 510(k) number is K941465.

When did SUTURE REMOVAL KIT receive FDA 510(k) clearance?

SUTURE REMOVAL KIT received FDA 510(k) clearance on 1994-04-22, under 510(k) number K941465.

Who is the listed applicant for SUTURE REMOVAL KIT?

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

What is the FDA product code for SUTURE REMOVAL KIT?

The FDA product code for SUTURE REMOVAL KIT is MCZ.

Related Clinical Trials

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.

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Other records listing Clinical Resources, 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.

K941470TRACHEOSTOMY CARE KITK944882IRRIGATION TRAYK944881SKIN SCRUB TRAYK945020FLUFF GAUZE SPONGEK945019FLUFF GAUXZE ROLLK945021FLUFF GAUZE SPONGE

View all 14 devices →

Related Devices (Code: MCZ)

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.

K050656AMSINO SUTURE REMOVAL KITAmsino International, Inc.K964827PROD. NO. 01-132 - SUTURE REMOVAL KITContinental Medical Laboratories, Inc.K963714GRAND MEDICAL SUTURE REMOVAL KITGrand Medical ProductsK943046SKIN STAPLE REMOVAL TRAYSSterile Concepts, Inc.K931597CARAPACE INCISION AND DRAINAGE TRAYSCarapace, Inc.K925015STERILE SUTURE REMOVAL KITCustomed, 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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