510(k) K822755
K822755 is an FDA 510(k) premarket notification submitted by American Hospital Supply Corp. for the device "LATEX PENROSE TUBING". The FDA issued a decision of Substantially Equivalent on January 21, 1983. American Hospital Supply Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 21, 1983
- Date Received
- September 8, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No