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FDA 510(k)

MODEL GP-252 GENERAL PURPOSE COIL

K-Number: K935691 · 1994-08-01

ApplicantDiagnostic Instrument Corp.
Decision Date1994-08-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL GP-252 GENERAL PURPOSE COIL is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Instrument Corp.. It received FDA 510(k) clearance on 1994-08-01 under 510(k) number K935691. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL GP-252 GENERAL PURPOSE COIL?

MODEL GP-252 GENERAL PURPOSE COIL is a medical device that received FDA 510(k) clearance on 1994-08-01. The listed applicant is Diagnostic Instrument Corp.. The 510(k) number is K935691.

When did MODEL GP-252 GENERAL PURPOSE COIL receive FDA 510(k) clearance?

MODEL GP-252 GENERAL PURPOSE COIL received FDA 510(k) clearance on 1994-08-01, under 510(k) number K935691.

Who is the listed applicant for MODEL GP-252 GENERAL PURPOSE COIL?

The FDA 510(k) record lists Diagnostic Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL GP-252 GENERAL PURPOSE COIL?

The FDA product code for MODEL GP-252 GENERAL PURPOSE COIL is LNH.

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Other records listing Diagnostic Instrument Corp. 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.

K934318DIAGNOSTIC INSTRUMLENTS INC. MODEL T803 BREAST COIL

Related Devices (Code: LNH)

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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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