FDA 510(k)

INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA

K-Number: K911316 · 1991-04-29

Decision Date1991-04-29

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA 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 1991-04-29 under 510(k) number K911316. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA?

INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA is a medical device that received FDA 510(k) clearance on 1991-04-29. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K911316.

When did INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA receive FDA 510(k) clearance?

INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA received FDA 510(k) clearance on 1991-04-29, under 510(k) number K911316.

Who is the listed applicant for INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA?

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 INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA?

The FDA product code for INSULATED HOOK SCISSORS/J & L HOOK KNIVES/SPATULA is GEI.

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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.