FDA 510(k)

WIRE TWISTERS

K-Number: K844147 · 1984-11-20

Decision Date1984-11-20

Product Code

DecisionSubstantially Equivalent

Device Summary

WIRE TWISTERS 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 1984-11-20 under 510(k) number K844147. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WIRE TWISTERS?

WIRE TWISTERS is a medical device that received FDA 510(k) clearance on 1984-11-20. The listed applicant is Med-Tool, Inc.. The 510(k) number is K844147.

When did WIRE TWISTERS receive FDA 510(k) clearance?

WIRE TWISTERS received FDA 510(k) clearance on 1984-11-20, under 510(k) number K844147.

Who is the listed applicant for WIRE TWISTERS?

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

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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

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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.