510(k) K780279
K780279 is an FDA 510(k) premarket notification submitted by Nice-Pak Products, Inc. for the device "ICE-PAK, PDI". The FDA issued a decision of Substantially Equivalent on April 10, 1978. The device falls under product code IMD (Pack, Hot Or Cold, Disposable), a Class I device regulated under 21 CFR 890.5710. Nice-Pak Products, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 10, 1978
- Date Received
- February 21, 1978
- 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