510(k) K803048
K803048 is an FDA 510(k) premarket notification submitted by Vance Products, Inc. for the device "VANCE UROSTOMY APPLIANCE". The FDA issued a decision of Substantially Equivalent on December 22, 1980. The device falls under product code EXB (Collector, Ostomy), a Class I device regulated under 21 CFR 876.5900. Vance Products, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 22, 1980
- Date Received
- December 1, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Collector, Ostomy
- Device Class
- Class I
- Regulation Number
- 876.5900
- Review Panel
- GU
- Submission Type