510(k) K770729

PYELOSCOPE SYSTEM by Richard Wolf Medical Instruments Corp. — Product Code FGA

K770729 is an FDA 510(k) premarket notification submitted by Richard Wolf Medical Instruments Corp. for the device "PYELOSCOPE SYSTEM". The FDA issued a decision of Substantially Equivalent on April 28, 1977. The device falls under product code FGA (Kit, Nephroscope), a Class II device regulated under 21 CFR 876.1500. Richard Wolf Medical Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 28, 1977
Date Received
April 20, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Nephroscope
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type