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FDA 510(k)

VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560

K-Number: K924835 · 1993-03-23

ApplicantAmerican Healthcare Supply Co., Inc.
Decision Date1993-03-23
Product CodeMCZ
Advisory CommitteeSU
DecisionUnknown

Device Summary

VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560 is the device name listed in this FDA 510(k) record. The listed applicant is American Healthcare Supply Co., Inc.. It received FDA 510(k) clearance on 1993-03-23 under 510(k) number K924835. The device is classified under product code MCZ. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560?

VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560 is a medical device that received FDA 510(k) clearance on 1993-03-23. The listed applicant is American Healthcare Supply Co., Inc.. The 510(k) number is K924835.

When did VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560 receive FDA 510(k) clearance?

VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560 received FDA 510(k) clearance on 1993-03-23, under 510(k) number K924835.

Who is the listed applicant for VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560?

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

What is the FDA product code for VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560?

The FDA product code for VALU-PAK STERILE SUTURE REMOVAL KIT (AHC-50-549560 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 American Healthcare Supply Co., 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.

K925214SHAVE PREP TRAYS (NON-STERILE)K925216STERILE SKIN SCRUB TRAYSK925215STERILE SURGICAL INSTRUMENT TRAYSK924834PREMIERE STERILE SUTURE REMOVAL KIT(HC-50-54957)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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