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FDA 510(k)

TECHNICON BGII ANALYZER

K-Number: K780716 · 1978-06-14

ApplicantTechnicon Instruments Corp.
Decision Date1978-06-14
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECHNICON BGII ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1978-06-14 under 510(k) number K780716. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON BGII ANALYZER?

TECHNICON BGII ANALYZER is a medical device that received FDA 510(k) clearance on 1978-06-14. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K780716.

When did TECHNICON BGII ANALYZER receive FDA 510(k) clearance?

TECHNICON BGII ANALYZER received FDA 510(k) clearance on 1978-06-14, under 510(k) number K780716.

Who is the listed applicant for TECHNICON BGII ANALYZER?

The FDA 510(k) record lists Technicon Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TECHNICON BGII ANALYZER?

The FDA product code for TECHNICON BGII ANALYZER is CHL.

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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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