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FDA 510(k)

BICHROMATIC ANALYZER ABA-200

K-Number: K771345 · 1977-08-04

ApplicantAbbott Laboratories
Decision Date1977-08-04
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BICHROMATIC 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 1977-08-04 under 510(k) number K771345. 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 BICHROMATIC ANALYZER ABA-200?

BICHROMATIC ANALYZER ABA-200 is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Abbott Laboratories. The 510(k) number is K771345.

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

BICHROMATIC ANALYZER ABA-200 received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771345.

Who is the listed applicant for BICHROMATIC 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 BICHROMATIC ANALYZER ABA-200?

The FDA product code for BICHROMATIC 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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