510(k) K840475

CYSTOTOME, 140-S by Cilco, Inc. — Product Code HNY

K840475 is an FDA 510(k) premarket notification submitted by Cilco, Inc. for the device "CYSTOTOME, 140-S". The FDA issued a decision of Substantially Equivalent on April 5, 1984. The device falls under product code HNY (Cystotome), a Class I device regulated under 21 CFR 886.4350. Cilco, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 5, 1984
Date Received
February 3, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cystotome
Device Class
Class I
Regulation Number
886.4350
Review Panel
OP
Submission Type