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FDA 510(k)

TISSUE FORCEPS

K-Number: K831663 · 1983-09-26

ApplicantMedcare Products
Decision Date1983-09-26
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TISSUE 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 1983-09-26 under 510(k) number K831663. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSUE FORCEPS?

TISSUE FORCEPS is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Medcare Products. The 510(k) number is K831663.

When did TISSUE FORCEPS receive FDA 510(k) clearance?

TISSUE FORCEPS received FDA 510(k) clearance on 1983-09-26, under 510(k) number K831663.

Who is the listed applicant for TISSUE 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 TISSUE FORCEPS?

The FDA product code for TISSUE FORCEPS is KOC.

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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 RAZORK831665DISPOSABLE NEEDLE HOLDERK831664PLASTIC THUMB FORCEPS

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Related Devices (Code: KOC)

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.

K242479BLOOD TUBING LINES FOR HEMODIALYSIS AL Series (Archloop) BLOOD TUBING LINES FOR HEMODIALYSIS C18 Series AL-ADC-PU, AL-CDC-PU, C18RDC-PU, C18BDD-PU, C18SFD-PUNIKKISO CO., LTD.K242176BLOOD TUBING LINES FOR HEMODIALYSIS AL Series (Archloop) BLOOD TUBING LINES FOR HEMODIALYSIS C18 Series (AL-ADC-E(U), AL-CDC-E(U), C18RDC-E(U), C18BDD-E(U), C18SFD-E(U)NIKKISO CO., LTD.K231589Blood Tubing Lines for Hemodialysis AV06C-ENIKKISO CO., LTD.K230514Blood Tubing Lines for Hemodialysis AL Series (Archloop), Blood Tubing Lines for Hemodialysis C18 SeriesNIKKISO CO., LTD.K201207CombiSet SMARTECH Hemodialysis Blood Tubing Set with attached Priming Set and Integrated Crit-Line Technology, CombiSet SMARTECH Hemodialysis Blood Tubing Set with attached Priming Set and Intergrated Crit-Line Technology, no Heparin LineFresenius Medical Care Renal Therapies Group, LLCK172238CAREline Airless Hemodialysis Blood Tubing SetsFresenius Medical Care Renal Therapies Group, LLC

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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