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FDA 510(k)

FMS-02 FLOOR-UNIT MODEL MICROSCOPE

K-Number: K802713 · 1980-11-19

Decision Date1980-11-19
Product CodeFSO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FMS-02 FLOOR-UNIT MODEL MICROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Jedmed Instrument Co.. It received FDA 510(k) clearance on 1980-11-19 under 510(k) number K802713. The device is classified under product code FSO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FMS-02 FLOOR-UNIT MODEL MICROSCOPE?

FMS-02 FLOOR-UNIT MODEL MICROSCOPE is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K802713.

When did FMS-02 FLOOR-UNIT MODEL MICROSCOPE receive FDA 510(k) clearance?

FMS-02 FLOOR-UNIT MODEL MICROSCOPE received FDA 510(k) clearance on 1980-11-19, under 510(k) number K802713.

Who is the listed applicant for FMS-02 FLOOR-UNIT MODEL MICROSCOPE?

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

What is the FDA product code for FMS-02 FLOOR-UNIT MODEL MICROSCOPE?

The FDA product code for FMS-02 FLOOR-UNIT MODEL MICROSCOPE is FSO.

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 Jedmed Instrument 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 91 devices →

Related Devices (Code: FSO)

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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