510(k) K926217
K926217 is an FDA 510(k) premarket notification submitted by Terumo Medical Corp. for the device "TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE". The FDA issued a decision of Substantially Equivalent on July 13, 1993. The device falls under product code GBZ (Catheter, Cholangiography), a Class I device regulated under 21 CFR 878.4200. Terumo Medical Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 13, 1993
- Date Received
- December 10, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Cholangiography
- Device Class
- Class I
- Regulation Number
- 878.4200
- Review Panel
- SU
- Submission Type