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FDA 510(k)

C RING CLINCHER

K-Number: K781446 · 1978-09-27

ApplicantOrthopedic Equipment Co., Inc.
Decision Date1978-09-27
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

C RING CLINCHER is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1978-09-27 under 510(k) number K781446. 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 C RING CLINCHER?

C RING CLINCHER is a medical device that received FDA 510(k) clearance on 1978-09-27. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K781446.

When did C RING CLINCHER receive FDA 510(k) clearance?

C RING CLINCHER received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781446.

Who is the listed applicant for C RING CLINCHER?

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

What is the FDA product code for C RING CLINCHER?

The FDA product code for C RING CLINCHER is GEN.

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Other records listing Orthopedic Equipment Co., Inc. 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.

K834035UNIVERSAL SELF-ALIGNING ACETABULAR COMK841189OEC/REZAIAN SPINAL FIXATORK800530SCHLEIN TRI-SURFACE ANKLEK781445SPREADERK790247TOURNIQUET TEST GAGEK790209FILTER SYSTEM, ALTNER DISPOSABLE

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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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