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FDA 510(k)

MICROFLUOR B PLATE & MICRO FLUOR W PLATE

K-Number: K822960 · 1982-11-16

Decision Date1982-11-16
Product CodeLIB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MICROFLUOR B PLATE & MICRO FLUOR W PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Corp.. It received FDA 510(k) clearance on 1982-11-16 under 510(k) number K822960. The device is classified under product code LIB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROFLUOR B PLATE & MICRO FLUOR W PLATE?

MICROFLUOR B PLATE & MICRO FLUOR W PLATE is a medical device that received FDA 510(k) clearance on 1982-11-16. The listed applicant is Dynatech Corp.. The 510(k) number is K822960.

When did MICROFLUOR B PLATE & MICRO FLUOR W PLATE receive FDA 510(k) clearance?

MICROFLUOR B PLATE & MICRO FLUOR W PLATE received FDA 510(k) clearance on 1982-11-16, under 510(k) number K822960.

Who is the listed applicant for MICROFLUOR B PLATE & MICRO FLUOR W PLATE?

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 MICROFLUOR B PLATE & MICRO FLUOR W PLATE?

The FDA product code for MICROFLUOR B PLATE & MICRO FLUOR W PLATE is LIB.

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: LIB)

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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