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FDA 510(k)

JEDMED COMPACT ENDOSCOPIC BEAMSPLITTER

K-Number: K935247 · 1994-02-18

Decision Date1994-02-18
Product CodeFEA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

JEDMED COMPACT ENDOSCOPIC BEAMSPLITTER 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 1994-02-18 under 510(k) number K935247. The device is classified under product code FEA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JEDMED COMPACT ENDOSCOPIC BEAMSPLITTER?

JEDMED COMPACT ENDOSCOPIC BEAMSPLITTER is a medical device that received FDA 510(k) clearance on 1994-02-18. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K935247.

When did JEDMED COMPACT ENDOSCOPIC BEAMSPLITTER receive FDA 510(k) clearance?

JEDMED COMPACT ENDOSCOPIC BEAMSPLITTER received FDA 510(k) clearance on 1994-02-18, under 510(k) number K935247.

Who is the listed applicant for JEDMED COMPACT ENDOSCOPIC BEAMSPLITTER?

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 JEDMED COMPACT ENDOSCOPIC BEAMSPLITTER?

The FDA product code for JEDMED COMPACT ENDOSCOPIC BEAMSPLITTER is FEA.

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: FEA)

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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