FDA 510(k)

DOUBLE ACTION PIN CUTTER

K-Number: K851896 · 1985-05-21

Decision Date1985-05-21

Product Code

DecisionSubstantially Equivalent

Device Summary

DOUBLE ACTION PIN CUTTER 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 1985-05-21 under 510(k) number K851896. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOUBLE ACTION PIN CUTTER?

DOUBLE ACTION PIN CUTTER is a medical device that received FDA 510(k) clearance on 1985-05-21. The listed applicant is Med-Tool, Inc.. The 510(k) number is K851896.

When did DOUBLE ACTION PIN CUTTER receive FDA 510(k) clearance?

DOUBLE ACTION PIN CUTTER received FDA 510(k) clearance on 1985-05-21, under 510(k) number K851896.

Who is the listed applicant for DOUBLE ACTION PIN CUTTER?

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

Related Clinical Trials

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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Other records listing Med-Tool, Inc. as applicant

K874357TAPERED PUNCH K874359ADJUSTABLE WRENCHES K874356PIN PUNCH K874358COMBINATION WRENCHES K872388NAIL SET K872385VICE OR BENCH VICE

View all 28 devices →

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.