510(k) K953542
K953542 is an FDA 510(k) premarket notification submitted by Prism Technologies, Inc. for the device "COLDGEL". The FDA issued a decision of SN on October 30, 1995. The device falls under product code IMD (Pack, Hot Or Cold, Disposable), a Class I device regulated under 21 CFR 890.5710. Prism Technologies, Inc. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- October 30, 1995
- Date Received
- July 28, 1995
- 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