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FDA 510(k)

LASER IMMUNONEPHELOMETRIC ANALYZER

K-Number: K772361 · 1978-01-30

Decision Date1978-01-30
Product CodeJQX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LASER IMMUNONEPHELOMETRIC ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1978-01-30 under 510(k) number K772361. The device is classified under product code JQX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASER IMMUNONEPHELOMETRIC ANALYZER?

LASER IMMUNONEPHELOMETRIC ANALYZER is a medical device that received FDA 510(k) clearance on 1978-01-30. The listed applicant is G.D. Searle and Co.. The 510(k) number is K772361.

When did LASER IMMUNONEPHELOMETRIC ANALYZER receive FDA 510(k) clearance?

LASER IMMUNONEPHELOMETRIC ANALYZER received FDA 510(k) clearance on 1978-01-30, under 510(k) number K772361.

Who is the listed applicant for LASER IMMUNONEPHELOMETRIC ANALYZER?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LASER IMMUNONEPHELOMETRIC ANALYZER?

The FDA product code for LASER IMMUNONEPHELOMETRIC ANALYZER is JQX.

Related Clinical Trials

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.

Other records listing G.D. Searle and Co. as applicant

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.

View all 56 devices →

Related Devices (Code: JQX)

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.

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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