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FDA 510(k)

INTEGRATED DIGITAL MEDICAL RECORD (IDMR)

K-Number: K993338 · 1999-12-29

ApplicantIbm Israel , Ltd.
Decision Date1999-12-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTEGRATED DIGITAL MEDICAL RECORD (IDMR) is the device name listed in this FDA 510(k) record. The listed applicant is Ibm Israel , Ltd.. It received FDA 510(k) clearance on 1999-12-29 under 510(k) number K993338. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTEGRATED DIGITAL MEDICAL RECORD (IDMR)?

INTEGRATED DIGITAL MEDICAL RECORD (IDMR) is a medical device that received FDA 510(k) clearance on 1999-12-29. The listed applicant is Ibm Israel , Ltd.. The 510(k) number is K993338.

When did INTEGRATED DIGITAL MEDICAL RECORD (IDMR) receive FDA 510(k) clearance?

INTEGRATED DIGITAL MEDICAL RECORD (IDMR) received FDA 510(k) clearance on 1999-12-29, under 510(k) number K993338.

Who is the listed applicant for INTEGRATED DIGITAL MEDICAL RECORD (IDMR)?

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

What is the FDA product code for INTEGRATED DIGITAL MEDICAL RECORD (IDMR)?

The FDA product code for INTEGRATED DIGITAL MEDICAL RECORD (IDMR) is LLZ.

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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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