NEPHELOMETER, MIC-2000 LASER
K-Number: K790103 · 1979-03-12
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Device Summary
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.
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
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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