510(k) K963666
K963666 is an FDA 510(k) premarket notification submitted by Kick Ice, Inc. for the device "INSTANT COLD PACK". The FDA issued a decision of Substantially Equivalent on October 30, 1996. The device falls under product code IMD (Pack, Hot Or Cold, Disposable), a Class I device regulated under 21 CFR 890.5710. Kick Ice, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 30, 1996
- Date Received
- September 13, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pack, Hot Or Cold, Disposable
- Device Class
- Class I
- Regulation Number
- 890.5710
- Review Panel
- PM
- Submission Type