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FDA 510(k)

STERILE SUTURE REMOVAL KIT

K-Number: K925015 · 1993-06-07

ApplicantCustomed, Inc.
Decision Date1993-06-07
Product CodeMCZ
Advisory CommitteeSU
DecisionUnknown

Device Summary

STERILE SUTURE REMOVAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Customed, Inc.. It received FDA 510(k) clearance on 1993-06-07 under 510(k) number K925015. 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 STERILE SUTURE REMOVAL KIT?

STERILE SUTURE REMOVAL KIT is a medical device that received FDA 510(k) clearance on 1993-06-07. The listed applicant is Customed, Inc.. The 510(k) number is K925015.

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

STERILE SUTURE REMOVAL KIT received FDA 510(k) clearance on 1993-06-07, under 510(k) number K925015.

Who is the listed applicant for STERILE SUTURE REMOVAL KIT?

The FDA 510(k) record lists Customed, Inc. 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.

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Other records listing Customed, 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.

K974647FANFOLD DRAPE 41 X 57 PRODUCT NO. 900-633, RECORDER NO. 0633K971920GOWN POLY REINFORCED LARGE(PRODUCT NO.900-522)/(REORDER NO. 0522)K964011SUCTION CATHETER TRAY PRODUCT NO. 900277K962652URINARY DRAINAGE BAG, (REORDER NO. 0749 - PRODUCT NO. 900-749)K962596CUSTOMED BLOOD EXTRACTION KITK961442UNIVERSAL DRAINAGE TRAY

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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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