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FDA 510(k)

DISPOSABLE SKIN STAPLE REMOVER

K-Number: K920283 · 1992-05-22

ApplicantTrinity Laboratories, Inc.
Decision Date1992-05-22
Product CodeMCZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SKIN STAPLE REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Trinity Laboratories, Inc.. It received FDA 510(k) clearance on 1992-05-22 under 510(k) number K920283. 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 DISPOSABLE SKIN STAPLE REMOVER?

DISPOSABLE SKIN STAPLE REMOVER is a medical device that received FDA 510(k) clearance on 1992-05-22. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K920283.

When did DISPOSABLE SKIN STAPLE REMOVER receive FDA 510(k) clearance?

DISPOSABLE SKIN STAPLE REMOVER received FDA 510(k) clearance on 1992-05-22, under 510(k) number K920283.

Who is the listed applicant for DISPOSABLE SKIN STAPLE REMOVER?

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

What is the FDA product code for DISPOSABLE SKIN STAPLE REMOVER?

The FDA product code for DISPOSABLE SKIN STAPLE REMOVER is MCZ.

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Other records listing Trinity Laboratories, 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.

K981441HEART CATH TRAY, STERILE, DISPOSABLEK974238DENTAL TRAY, STERILE, DISPOSABLEK974286CIRCUMCISION TRAY, CAT. NO. 70340K972160CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE AGGLUTNATION LATEX TESTK970722EYE TRAYK965201O.R. SCRUB PREP TRAY, STERILE, DISPOSABLE

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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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