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FDA 510(k)

BLOCK(TM) ARTHROSCOPIC TOOL KIT

K-Number: K946174 · 1995-09-14

ApplicantJohnson
Decision Date1995-09-14
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BLOCK(TM) ARTHROSCOPIC TOOL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Johnson. It received FDA 510(k) clearance on 1995-09-14 under 510(k) number K946174. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOCK(TM) ARTHROSCOPIC TOOL KIT?

BLOCK(TM) ARTHROSCOPIC TOOL KIT is a medical device that received FDA 510(k) clearance on 1995-09-14. The listed applicant is Johnson. The 510(k) number is K946174.

When did BLOCK(TM) ARTHROSCOPIC TOOL KIT receive FDA 510(k) clearance?

BLOCK(TM) ARTHROSCOPIC TOOL KIT received FDA 510(k) clearance on 1995-09-14, under 510(k) number K946174.

Who is the listed applicant for BLOCK(TM) ARTHROSCOPIC TOOL KIT?

The FDA 510(k) record lists Johnson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOCK(TM) ARTHROSCOPIC TOOL KIT?

The FDA product code for BLOCK(TM) ARTHROSCOPIC TOOL KIT is HRX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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