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FDA 510(k)

VICE OR BENCH VICE

K-Number: K872385 · 1987-07-16

ApplicantMed-Tool, Inc.
Decision Date1987-07-16
Product CodeLSA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VICE OR BENCH VICE 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 1987-07-16 under 510(k) number K872385. The device is classified under product code LSA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VICE OR BENCH VICE?

VICE OR BENCH VICE is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Med-Tool, Inc.. The 510(k) number is K872385.

When did VICE OR BENCH VICE receive FDA 510(k) clearance?

VICE OR BENCH VICE received FDA 510(k) clearance on 1987-07-16, under 510(k) number K872385.

Who is the listed applicant for VICE OR BENCH VICE?

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 VICE OR BENCH VICE?

The FDA product code for VICE OR BENCH VICE is LSA.

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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 SETK872387STANDARD SCREW DRIVER

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.

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