FDA 510(k)

CAT 10-NEUROLOGY DEVICE

K-Number: K840314 · 1984-02-23

Decision Date1984-02-23

Product CodeGWZ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CAT 10-NEUROLOGY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Imm Enterprises , Ltd.. It received FDA 510(k) clearance on 1984-02-23 under 510(k) number K840314. The device is classified under product code GWZ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAT 10-NEUROLOGY DEVICE?

CAT 10-NEUROLOGY DEVICE is a medical device that received FDA 510(k) clearance on 1984-02-23. The listed applicant is Imm Enterprises , Ltd.. The 510(k) number is K840314.

When did CAT 10-NEUROLOGY DEVICE receive FDA 510(k) clearance?

CAT 10-NEUROLOGY DEVICE received FDA 510(k) clearance on 1984-02-23, under 510(k) number K840314.

Who is the listed applicant for CAT 10-NEUROLOGY DEVICE?

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

What is the FDA product code for CAT 10-NEUROLOGY DEVICE?

The FDA product code for CAT 10-NEUROLOGY DEVICE is GWZ.

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Other records listing Imm Enterprises , Ltd. as applicant

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Related Devices (Code: GWZ)

K891571PERCUSSION HAMMERSandal Surgico K852716TAYLOR PERCUSSION HAMMER SS 410 OR 420The Huxley Instrument Corp.K8517481/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINEArtiberia K834170OP-CON SURG. INSTRUMENT #10Imm Enterprises , Ltd.K834178H.R. JAKOBI SURG. INSTR. #10 34/36Imm Enterprises , Ltd.K810054RICA (DIAGNOSTIC INSTRUMENTS)Robert I. Chien & Assoc., Inc.

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.