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FDA 510(k)

AUTOMATIC ANALYZER

K-Number: K771662 · 1977-12-06

ApplicantLachat Chemicals, Inc.
Decision Date1977-12-06
Product CodeJJC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Lachat Chemicals, Inc.. It received FDA 510(k) clearance on 1977-12-06 under 510(k) number K771662. The device is classified under product code JJC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC ANALYZER?

AUTOMATIC ANALYZER is a medical device that received FDA 510(k) clearance on 1977-12-06. The listed applicant is Lachat Chemicals, Inc.. The 510(k) number is K771662.

When did AUTOMATIC ANALYZER receive FDA 510(k) clearance?

AUTOMATIC ANALYZER received FDA 510(k) clearance on 1977-12-06, under 510(k) number K771662.

Who is the listed applicant for AUTOMATIC ANALYZER?

The FDA 510(k) record lists Lachat Chemicals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOMATIC ANALYZER?

The FDA product code for AUTOMATIC ANALYZER is JJC.

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Related Devices (Code: JJC)

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.

K945915AVL OMNI ANALYZERAvl Scientific Corp.K945584NOVA 16 ANALYZERNova Biomedical Corp.K943376OPERA SYSTEMMiles, Inc.K901410TECHNICON RA-2000(TM) SYSTEMTechnicon Instruments Corp.K901141PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZXBaxter Healthcare CorpK890332RFA/2 RAPID FLOW ANALYZER W/COMPUTERAlpkem Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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