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FDA 510(k)

MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM

K-Number: K911158 · 1991-03-29

Decision Date1991-03-29
Product CodeLRW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM is the device name listed in this FDA 510(k) record. The listed applicant is Northgate Technologies, Inc.. It received FDA 510(k) clearance on 1991-03-29 under 510(k) number K911158. The device is classified under product code LRW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM?

MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K911158.

When did MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM receive FDA 510(k) clearance?

MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM received FDA 510(k) clearance on 1991-03-29, under 510(k) number K911158.

Who is the listed applicant for MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM?

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

What is the FDA product code for MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM?

The FDA product code for MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM is LRW.

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.

Other records listing Northgate Technologies, 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.

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Related Devices (Code: LRW)

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.

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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