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FDA 510(k)

ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTER

K-Number: K900160 · 1990-01-24

ApplicantJedmed Instrument Co.
Decision Date1990-01-24
Product CodeKQM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADAPTOR: KAPS CINE TO MOELLER 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 1990-01-24 under 510(k) number K900160. The device is classified under product code KQM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTER?

ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTER is a medical device that received FDA 510(k) clearance on 1990-01-24. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K900160.

When did ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTER receive FDA 510(k) clearance?

ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTER received FDA 510(k) clearance on 1990-01-24, under 510(k) number K900160.

Who is the listed applicant for ADAPTOR: KAPS CINE TO MOELLER 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 ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTER?

The FDA product code for ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTER is KQM.

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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.

K021750LID CHAIN EYELID WEIGHTSK954184JED-LIGHT FIBEROPTIC LIGHT SOURCEK944032VIDEO SCOPE SYSTEM (LARYNGOSCOPE)K953457JEDMED SPECTRUM ENT CABINETK950925JEDMED LARYNGEAL SCOPEK950785HORTMANN AIRMATIC AIR CALORIC STIMULATOR

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Related Devices (Code: KQM)

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.

K890826SONY VIDEO GRAPHIC PRINTER UP-850Sony Corp. of AmericaK885042SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MDSony Medical Electronics Co.K882958SONY VIDEO PRINTERS, UP SERIESSony Medical Electronics Co.K882924MEDICAM MC-7 AND RP-7 SURGICAL CAMERASM.P. Video, Inc.K873419VIDEO PRINTER SYSTEMTechnology For Imaging, Inc.K871595SURGICAL CAMERA ACCESSORIESM.P. Video, Inc.

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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