510(k) K790244

CYSTOTOMES by Visitec Co. — Product Code HNY

K790244 is an FDA 510(k) premarket notification submitted by Visitec Co. for the device "CYSTOTOMES". The FDA issued a decision of Substantially Equivalent on February 12, 1979. The device falls under product code HNY (Cystotome), a Class I device regulated under 21 CFR 886.4350. Visitec Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 12, 1979
Date Received
December 29, 1978
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