510(k) K960099

PENROSE DRAIN MODELS 6001 - 6007 by Sil-Med Corp. — Product Code GCY

K960099 is an FDA 510(k) premarket notification submitted by Sil-Med Corp. for the device "PENROSE DRAIN MODELS 6001 - 6007". The FDA issued a decision of Substantially Equivalent on March 11, 1996. The device falls under product code GCY (Apparatus, Suction, Single Patient Use, Portable, Nonpowered), a Class I device regulated under 21 CFR 878.4680. Sil-Med Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 11, 1996
Date Received
January 11, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apparatus, Suction, Single Patient Use, Portable, Nonpowered
Device Class
Class I
Regulation Number
878.4680
Review Panel
SU
Submission Type