510(k) K912885

KAPS 90 DEGREE FIBEROPTIC ADAPTOR by Jedmed Instrument Co. — Product Code EQH

K912885 is an FDA 510(k) premarket notification submitted by Jedmed Instrument Co. for the device "KAPS 90 DEGREE FIBEROPTIC ADAPTOR". The FDA issued a decision of Substantially Equivalent on August 30, 1991. The device falls under product code EQH (Source, Carrier, Fiberoptic Light), a Class I device regulated under 21 CFR 874.4350. Jedmed Instrument Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 30, 1991
Date Received
July 1, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Source, Carrier, Fiberoptic Light
Device Class
Class I
Regulation Number
874.4350
Review Panel
EN
Submission Type