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FDA 510(k)

DIAGNOSTIC INSTRUMLENTS INC. MODEL T803 BREAST COIL

K-Number: K934318 · 1994-08-22

ApplicantDiagnostic Instrument Corp.
Decision Date1994-08-22
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIAGNOSTIC INSTRUMLENTS INC. MODEL T803 BREAST 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 1994-08-22 under 510(k) number K934318. 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 DIAGNOSTIC INSTRUMLENTS INC. MODEL T803 BREAST COIL?

DIAGNOSTIC INSTRUMLENTS INC. MODEL T803 BREAST COIL is a medical device that received FDA 510(k) clearance on 1994-08-22. The listed applicant is Diagnostic Instrument Corp.. The 510(k) number is K934318.

When did DIAGNOSTIC INSTRUMLENTS INC. MODEL T803 BREAST COIL receive FDA 510(k) clearance?

DIAGNOSTIC INSTRUMLENTS INC. MODEL T803 BREAST COIL received FDA 510(k) clearance on 1994-08-22, under 510(k) number K934318.

Who is the listed applicant for DIAGNOSTIC INSTRUMLENTS INC. MODEL T803 BREAST 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 DIAGNOSTIC INSTRUMLENTS INC. MODEL T803 BREAST COIL?

The FDA product code for DIAGNOSTIC INSTRUMLENTS INC. MODEL T803 BREAST COIL is LNH.

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.

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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.

K935691MODEL GP-252 GENERAL PURPOSE COIL

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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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Official Source

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