510(k) K830546
K830546 is an FDA 510(k) premarket notification submitted by American Hospital Supply Corp. for the device "DOSIMETRIC RELEASE". The FDA issued a decision of Substantially Equivalent on May 25, 1983. The device falls under product code KQT (Evacuator, Gastro-Urology), a Class II device regulated under 21 CFR 876.4370. American Hospital Supply Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 25, 1983
- Date Received
- February 22, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Evacuator, Gastro-Urology
- Device Class
- Class II
- Regulation Number
- 876.4370
- Review Panel
- GU
- Submission Type