Kaps 90 Degree Fiberoptic Adaptor

FDA 510(k) K912885 · Jedmed Instrument Co.

Substantially Equivalent

510(k) numberK912885

Submission

Device name
Kaps 90 Degree Fiberoptic Adaptor
Applicant
Jedmed Instrument Co.
St.Louis, MO, US
Received
July 1, 1991
Decision date
August 30, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
EQH – Source, Carrier, Fiberoptic Light
Device class
Class I (low risk)
Regulation
21 CFR 874.4350
Specialty
Ear, Nose, Throat

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Questions and answers

When was Kaps 90 Degree Fiberoptic Adaptor cleared by the FDA?

Kaps 90 Degree Fiberoptic Adaptor (K912885) received a 510(k) decision of Substantially Equivalent on August 30, 1991, 60 days after the submission was received.

What is the product code of K912885?

The FDA product code is EQH – Source, Carrier, Fiberoptic Light, a Class I (low risk) device regulated under 21 CFR 874.4350.