510(k) K862709

MECHANICAL CYSTITOME by Rudolph Beaver, Inc. — Product Code HNY

K862709 is an FDA 510(k) premarket notification submitted by Rudolph Beaver, Inc. for the device "MECHANICAL CYSTITOME". The FDA issued a decision of Substantially Equivalent on August 1, 1986. The device falls under product code HNY (Cystotome), a Class I device regulated under 21 CFR 886.4350. Rudolph Beaver, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 1, 1986
Date Received
July 16, 1986
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