510(k) K822755

LATEX PENROSE TUBING by American Hospital Supply Corp.

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