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FDA 510(k)

ADC-500 AUTOMATED DIFFER. CELL CNTR. SY.

K-Number: K803219 · 1981-01-21

ApplicantAbbott Laboratories
Decision Date1981-01-21
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ADC-500 AUTOMATED DIFFER. CELL CNTR. SY. is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1981-01-21 under 510(k) number K803219. The device is classified under product code GKZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADC-500 AUTOMATED DIFFER. CELL CNTR. SY.?

ADC-500 AUTOMATED DIFFER. CELL CNTR. SY. is a medical device that received FDA 510(k) clearance on 1981-01-21. The listed applicant is Abbott Laboratories. The 510(k) number is K803219.

When did ADC-500 AUTOMATED DIFFER. CELL CNTR. SY. receive FDA 510(k) clearance?

ADC-500 AUTOMATED DIFFER. CELL CNTR. SY. received FDA 510(k) clearance on 1981-01-21, under 510(k) number K803219.

Who is the listed applicant for ADC-500 AUTOMATED DIFFER. CELL CNTR. SY.?

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 ADC-500 AUTOMATED DIFFER. CELL CNTR. SY.?

The FDA product code for ADC-500 AUTOMATED DIFFER. CELL CNTR. SY. is GKZ.

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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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