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FDA 510(k)

PROBES,SCISSORS,FORCEPS,GRASPERS,&NEEDLE HOLDERS

K-Number: K933067 · 1994-01-27

ApplicantMedline Industries, Inc.
Decision Date1994-01-27
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PROBES,SCISSORS,FORCEPS,GRASPERS,&NEEDLE HOLDERS is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1994-01-27 under 510(k) number K933067. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROBES,SCISSORS,FORCEPS,GRASPERS,&NEEDLE HOLDERS?

PROBES,SCISSORS,FORCEPS,GRASPERS,&NEEDLE HOLDERS is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Medline Industries, Inc.. The 510(k) number is K933067.

When did PROBES,SCISSORS,FORCEPS,GRASPERS,&NEEDLE HOLDERS receive FDA 510(k) clearance?

PROBES,SCISSORS,FORCEPS,GRASPERS,&NEEDLE HOLDERS received FDA 510(k) clearance on 1994-01-27, under 510(k) number K933067.

Who is the listed applicant for PROBES,SCISSORS,FORCEPS,GRASPERS,&NEEDLE HOLDERS?

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

What is the FDA product code for PROBES,SCISSORS,FORCEPS,GRASPERS,&NEEDLE HOLDERS?

The FDA product code for PROBES,SCISSORS,FORCEPS,GRASPERS,&NEEDLE HOLDERS is GCJ.

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Related Devices (Code: GCJ)

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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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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