510(k) K960211

CPR TOTAL KNEE PACK by Custom Pack Reliability — Product Code FRG

K960211 is an FDA 510(k) premarket notification submitted by Custom Pack Reliability for the device "CPR TOTAL KNEE PACK". The FDA issued a decision of Substantially Equivalent on April 12, 1996. The device falls under product code FRG (Wrap, Sterilization), a Class II device regulated under 21 CFR 880.6850. Custom Pack Reliability has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 12, 1996
Date Received
January 16, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Wrap, Sterilization
Device Class
Class II
Regulation Number
880.6850
Review Panel
HO
Submission Type