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FDA 510(k)

C CLAMP

K-Number: K872386 · 1987-07-02

ApplicantMed-Tool, Inc.
Decision Date1987-07-02
Product CodeHXD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

C CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Med-Tool, Inc.. It received FDA 510(k) clearance on 1987-07-02 under 510(k) number K872386. The device is classified under product code HXD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C CLAMP?

C CLAMP is a medical device that received FDA 510(k) clearance on 1987-07-02. The listed applicant is Med-Tool, Inc.. The 510(k) number is K872386.

When did C CLAMP receive FDA 510(k) clearance?

C CLAMP received FDA 510(k) clearance on 1987-07-02, under 510(k) number K872386.

Who is the listed applicant for C CLAMP?

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

What is the FDA product code for C CLAMP?

The FDA product code for C CLAMP is HXD.

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Other records listing Med-Tool, 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.

K874357TAPERED PUNCHK874359ADJUSTABLE WRENCHESK874356PIN PUNCHK874358COMBINATION WRENCHESK872388NAIL SETK872385VICE OR BENCH VICE

View all 28 devices →

Related Devices (Code: HXD)

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.

K890371INTESTINAL CRUSHING CLAMPKinetic Medical ProductsK890372INTESTINAL CLAMPKinetic Medical ProductsK890381PARAMETRIUM CLAMPKinetic Medical ProductsK890368KIDNEY CLAMPKinetic Medical ProductsK874959VASCULAR CLAMPSolway, Inc.K863653SUCTION-OFFB&B Medical Technologies, 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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