510(k) K830026

FIBERSCOPE DISINFECTANT IRRIGATOR by Keymed, Inc. — Product Code FEB

K830026 is an FDA 510(k) premarket notification submitted by Keymed, Inc. for the device "FIBERSCOPE DISINFECTANT IRRIGATOR". The FDA issued a decision of Substantially Equivalent on January 14, 1983. The device falls under product code FEB (Accessories, Cleaning, For Endoscope), a Class II device regulated under 21 CFR 876.1500. Keymed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 14, 1983
Date Received
January 4, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Accessories, Cleaning, For Endoscope
Device Class
Class II
Regulation Number
876.1500
Review Panel
HO
Submission Type

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).