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FDA 510(k)

MARCUSE TUBE CLAMPING FORCEPS, STRAIGHT

K-Number: K761334 · 1977-02-24

ApplicantJ. Sklar Mfg. Co., Inc.
Decision Date1977-02-24
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MARCUSE TUBE CLAMPING FORCEPS, STRAIGHT is the device name listed in this FDA 510(k) record. The listed applicant is J. Sklar Mfg. Co., Inc.. It received FDA 510(k) clearance on 1977-02-24 under 510(k) number K761334. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARCUSE TUBE CLAMPING FORCEPS, STRAIGHT?

MARCUSE TUBE CLAMPING FORCEPS, STRAIGHT is a medical device that received FDA 510(k) clearance on 1977-02-24. The listed applicant is J. Sklar Mfg. Co., Inc.. The 510(k) number is K761334.

When did MARCUSE TUBE CLAMPING FORCEPS, STRAIGHT receive FDA 510(k) clearance?

MARCUSE TUBE CLAMPING FORCEPS, STRAIGHT received FDA 510(k) clearance on 1977-02-24, under 510(k) number K761334.

Who is the listed applicant for MARCUSE TUBE CLAMPING FORCEPS, STRAIGHT?

The FDA 510(k) record lists J. Sklar Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARCUSE TUBE CLAMPING FORCEPS, STRAIGHT?

The FDA product code for MARCUSE TUBE CLAMPING FORCEPS, STRAIGHT is GEN.

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Other records listing J. Sklar Mfg. Co., Inc. as applicant

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Related Devices (Code: GEN)

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.

K031828NATURALASE LP ND:YAG LASERFocus Medical, LLCK953962FORCEPSBiopsys Medical, Inc.K932385SUTURE REMOVING FORCEPSRocket of London, Ltd.K904723FORCEPSMinto Research & Development, Inc.K911159PALPATION PROBENorthgate Technologies, Inc.K900952GS-1200 GRASPING/EXTRACTING FORCEP, 10MMSolos Endoscopy, 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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