510(k) K813132
K813132 is an FDA 510(k) premarket notification submitted by Universal Prosthetics, Inc. for the device "THE CHICAGO GULLET". The FDA issued a decision of Substantially Equivalent on Jan 7, 1982. The device falls under product code KNT (Tubes, Gastrointestinal (And Accessories)), a Class II device regulated under 21 CFR 876.5980. Universal Prosthetics, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 7, 1982
- Date Received
- Nov 5, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tubes, Gastrointestinal (And Accessories)
- Device Class
- Class II
- Regulation Number
- 876.5980
- Review Panel
- GU
- Submission Type