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FDA 510(k)

OPERATING ROOM NEEDLE COUNTER

K-Number: K923512 · 1992-11-23

ApplicantSharp-Trap, Inc.
Decision Date1992-11-23
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OPERATING ROOM NEEDLE COUNTER is the device name listed in this FDA 510(k) record. The listed applicant is Sharp-Trap, Inc.. It received FDA 510(k) clearance on 1992-11-23 under 510(k) number K923512. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPERATING ROOM NEEDLE COUNTER?

OPERATING ROOM NEEDLE COUNTER is a medical device that received FDA 510(k) clearance on 1992-11-23. The listed applicant is Sharp-Trap, Inc.. The 510(k) number is K923512.

When did OPERATING ROOM NEEDLE COUNTER receive FDA 510(k) clearance?

OPERATING ROOM NEEDLE COUNTER received FDA 510(k) clearance on 1992-11-23, under 510(k) number K923512.

Who is the listed applicant for OPERATING ROOM NEEDLE COUNTER?

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

What is the FDA product code for OPERATING ROOM NEEDLE COUNTER?

The FDA product code for OPERATING ROOM NEEDLE COUNTER is MMK.

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Related Devices (Code: MMK)

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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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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