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FDA 510(k)

NEPHELOMETER, MIC-2000 LASER

K-Number: K790103 · 1979-03-12

Decision Date1979-03-12
Product CodeJQX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NEPHELOMETER, MIC-2000 LASER is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Corp.. It received FDA 510(k) clearance on 1979-03-12 under 510(k) number K790103. 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 NEPHELOMETER, MIC-2000 LASER?

NEPHELOMETER, MIC-2000 LASER is a medical device that received FDA 510(k) clearance on 1979-03-12. The listed applicant is Dynatech Corp.. The 510(k) number is K790103.

When did NEPHELOMETER, MIC-2000 LASER receive FDA 510(k) clearance?

NEPHELOMETER, MIC-2000 LASER received FDA 510(k) clearance on 1979-03-12, under 510(k) number K790103.

Who is the listed applicant for NEPHELOMETER, MIC-2000 LASER?

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

What is the FDA product code for NEPHELOMETER, MIC-2000 LASER?

The FDA product code for NEPHELOMETER, MIC-2000 LASER 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 Dynatech Corp. 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 27 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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