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FDA 510(k)

SPOON FORCEPS, 11MM

K-Number: K911364 · 1991-10-23

ApplicantNorthgate Technologies, Inc.
Decision Date1991-10-23
Product CodeLQC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SPOON FORCEPS, 11MM 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 1991-10-23 under 510(k) number K911364. The device is classified under product code LQC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPOON FORCEPS, 11MM?

SPOON FORCEPS, 11MM is a medical device that received FDA 510(k) clearance on 1991-10-23. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K911364.

When did SPOON FORCEPS, 11MM receive FDA 510(k) clearance?

SPOON FORCEPS, 11MM received FDA 510(k) clearance on 1991-10-23, under 510(k) number K911364.

Who is the listed applicant for SPOON FORCEPS, 11MM?

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 SPOON FORCEPS, 11MM?

The FDA product code for SPOON FORCEPS, 11MM is LQC.

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Related Devices (Code: LQC)

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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.

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