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FDA 510(k)

STERILE SUTURE REMOVAL KIT

K-Number: K812132 · 1981-12-01

ApplicantE.M. Adams
Decision Date1981-12-01
Product CodeMCZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE SUTURE REMOVAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is E.M. Adams. It received FDA 510(k) clearance on 1981-12-01 under 510(k) number K812132. 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 STERILE SUTURE REMOVAL KIT?

STERILE SUTURE REMOVAL KIT is a medical device that received FDA 510(k) clearance on 1981-12-01. The listed applicant is E.M. Adams. The 510(k) number is K812132.

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

STERILE SUTURE REMOVAL KIT received FDA 510(k) clearance on 1981-12-01, under 510(k) number K812132.

Who is the listed applicant for STERILE SUTURE REMOVAL KIT?

The FDA 510(k) record lists E.M. Adams as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE SUTURE REMOVAL KIT?

The FDA product code for STERILE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing E.M. Adams 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.

K905173SPLASH GUARDK910468STERILE DISPOSABLE DRAPE(S)K873978DISPOSABLE BIPOLAR FORCEPSK850063INSTRUMENT POCKETK843724I.V. START KIT & OBSTETRICAL KITK843783WET PACK

View all 21 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.K941465SUTURE REMOVAL KITClinical Resources, Inc.K931597CARAPACE INCISION AND DRAINAGE TRAYSCarapace, 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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