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FDA 510(k)

YBBOTT CMV TOTAL AB EIA

K-Number: K832221 · 1983-10-27

ApplicantAbbott Laboratories
Decision Date1983-10-27
Product CodeLFZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

YBBOTT CMV TOTAL AB EIA is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1983-10-27 under 510(k) number K832221. The device is classified under product code LFZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YBBOTT CMV TOTAL AB EIA?

YBBOTT CMV TOTAL AB EIA is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Abbott Laboratories. The 510(k) number is K832221.

When did YBBOTT CMV TOTAL AB EIA receive FDA 510(k) clearance?

YBBOTT CMV TOTAL AB EIA received FDA 510(k) clearance on 1983-10-27, under 510(k) number K832221.

Who is the listed applicant for YBBOTT CMV TOTAL AB EIA?

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

What is the FDA product code for YBBOTT CMV TOTAL AB EIA?

The FDA product code for YBBOTT CMV TOTAL AB EIA is LFZ.

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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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