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FDA 510(k)

IMEXDOP CT+

K-Number: K942441 · 1994-08-23

ApplicantImex Medical Systems, Inc.
Decision Date1994-08-23
Product CodeJAF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMEXDOP CT+ is the device name listed in this FDA 510(k) record. The listed applicant is Imex Medical Systems, Inc.. It received FDA 510(k) clearance on 1994-08-23 under 510(k) number K942441. The device is classified under product code JAF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMEXDOP CT+?

IMEXDOP CT+ is a medical device that received FDA 510(k) clearance on 1994-08-23. The listed applicant is Imex Medical Systems, Inc.. The 510(k) number is K942441.

When did IMEXDOP CT+ receive FDA 510(k) clearance?

IMEXDOP CT+ received FDA 510(k) clearance on 1994-08-23, under 510(k) number K942441.

Who is the listed applicant for IMEXDOP CT+?

The FDA 510(k) record lists Imex Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMEXDOP CT+?

The FDA product code for IMEXDOP CT+ is JAF.

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Other records listing Imex Medical Systems, Inc. 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.

K973556IMEX MEDICAL SYSTEMS, INC. IMEXLAB 9000K973562IMEX MEDICAL SYSTEMS, INC. IMEXLAB 9100K973336IMEX STETHODOPK970156IMEX FUTURALDOP PROK942243IMEX 8000 PERSONAL CASCULAR LABK944196IMWXDOP IR

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Related Devices (Code: JAF)

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.

K242487Laminar P1 (LDH-HW-001)Laminar Digital Health, Inc.K110628SIMPLEABINewman MedicalK093393LIFEDOP MODEL 300ABISummit Doppler Systems, Inc.K090009THD SLIDE ONEThd SpaK081429THD SLIDEThd SpaK070815THDG.F. S.R.L.

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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