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FDA 510(k)

ANALYZER ABA-200

K-Number: K782014 · 1979-01-10

ApplicantAbbott Laboratories
Decision Date1979-01-10
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANALYZER ABA-200 is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1979-01-10 under 510(k) number K782014. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALYZER ABA-200?

ANALYZER ABA-200 is a medical device that received FDA 510(k) clearance on 1979-01-10. The listed applicant is Abbott Laboratories. The 510(k) number is K782014.

When did ANALYZER ABA-200 receive FDA 510(k) clearance?

ANALYZER ABA-200 received FDA 510(k) clearance on 1979-01-10, under 510(k) number K782014.

Who is the listed applicant for ANALYZER ABA-200?

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 ANALYZER ABA-200?

The FDA product code for ANALYZER ABA-200 is JJE.

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Related Devices (Code: JJE)

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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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