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FDA 510(k)

SOM 6V

K-Number: K910357 · 1991-02-19

Decision Date1991-02-19
Product CodeFSO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SOM 6V 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 1991-02-19 under 510(k) number K910357. 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 SOM 6V?

SOM 6V is a medical device that received FDA 510(k) clearance on 1991-02-19. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K910357.

When did SOM 6V receive FDA 510(k) clearance?

SOM 6V received FDA 510(k) clearance on 1991-02-19, under 510(k) number K910357.

Who is the listed applicant for SOM 6V?

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 SOM 6V?

The FDA product code for SOM 6V is FSO.

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

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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