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FDA 510(k)

ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES

K-Number: K954052 · 1995-11-06

ApplicantT. Korossurgical Instruments Corp.
Decision Date1995-11-06
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES is the device name listed in this FDA 510(k) record. The listed applicant is T. Korossurgical Instruments Corp.. It received FDA 510(k) clearance on 1995-11-06 under 510(k) number K954052. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES?

ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES is a medical device that received FDA 510(k) clearance on 1995-11-06. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K954052.

When did ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES receive FDA 510(k) clearance?

ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES received FDA 510(k) clearance on 1995-11-06, under 510(k) number K954052.

Who is the listed applicant for ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES?

The FDA 510(k) record lists T. Korossurgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES?

The FDA product code for ARTHROSCOPIC GRASPER, CUP FORCEPS AND CURETTES is HRX.

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Other records listing T. Korossurgical Instruments Corp. as applicant

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Related Devices (Code: HRX)

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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