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FDA 510(k)

PLASTIC THUMB FORCEPS

K-Number: K831664 · 1983-09-12

ApplicantMedcare Products
Decision Date1983-09-12
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PLASTIC THUMB FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Medcare Products. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K831664. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASTIC THUMB FORCEPS?

PLASTIC THUMB FORCEPS is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Medcare Products. The 510(k) number is K831664.

When did PLASTIC THUMB FORCEPS receive FDA 510(k) clearance?

PLASTIC THUMB FORCEPS received FDA 510(k) clearance on 1983-09-12, under 510(k) number K831664.

Who is the listed applicant for PLASTIC THUMB FORCEPS?

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

What is the FDA product code for PLASTIC THUMB FORCEPS?

The FDA product code for PLASTIC THUMB FORCEPS is KDC.

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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 Medcare Products 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.

K841122TRACHEOSTOMY CARE TRAYK841124DIALYSIS TRAYK841123DRESSING CHANGE TRAYK831374MED CARE PREP RAZORK831663TISSUE FORCEPSK831665DISPOSABLE NEEDLE HOLDER

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Related Devices (Code: KDC)

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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. Concepts, 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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