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FDA 510(k)

PHYSICIAN'S DESKTOP REVIEW

K-Number: K021669 · 2002-06-05

ApplicantAdac Laboratories
Decision Date2002-06-05
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHYSICIAN'S DESKTOP REVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Adac Laboratories. It received FDA 510(k) clearance on 2002-06-05 under 510(k) number K021669. 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 PHYSICIAN'S DESKTOP REVIEW?

PHYSICIAN'S DESKTOP REVIEW is a medical device that received FDA 510(k) clearance on 2002-06-05. The listed applicant is Adac Laboratories. The 510(k) number is K021669.

When did PHYSICIAN'S DESKTOP REVIEW receive FDA 510(k) clearance?

PHYSICIAN'S DESKTOP REVIEW received FDA 510(k) clearance on 2002-06-05, under 510(k) number K021669.

Who is the listed applicant for PHYSICIAN'S DESKTOP REVIEW?

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

What is the FDA product code for PHYSICIAN'S DESKTOP REVIEW?

The FDA product code for PHYSICIAN'S DESKTOP REVIEW 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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