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FDA 510(k)

AUTO-LOGIC II SYSTEM

K-Number: K771129 · 1977-08-04

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

Device Summary

AUTO-LOGIC II SYSTEM 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 K771129. The device is classified under product code JJJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO-LOGIC II SYSTEM?

AUTO-LOGIC II SYSTEM 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 K771129.

When did AUTO-LOGIC II SYSTEM receive FDA 510(k) clearance?

AUTO-LOGIC II SYSTEM received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771129.

Who is the listed applicant for AUTO-LOGIC II SYSTEM?

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 AUTO-LOGIC II SYSTEM?

The FDA product code for AUTO-LOGIC II SYSTEM is JJJ.

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Related Devices (Code: JJJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K962762SEQUENTIAL SAMPLE MULTI-PHOTON DETECTORBiotraces, Inc.K946387CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTERCapintec, Inc.K920559ABBOTT VERTEX ANALYZERAbbott LaboratoriesK900087GENESYS 6000 GAMMA COUNTERLaboratory Technologies, Inc.K896202MATRIX(TM)-96Canberra Industries, Inc.K894902SOURCEREROakfield Instruments, Ltd.

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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