510(k) K932539
K932539 is an FDA 510(k) premarket notification submitted by Three Dog Down for the device "DOCTOR DOWN --RESCUE WRAP". The FDA issued a decision of Substantially Equivalent on November 2, 1993. The device falls under product code KME (Bedding, Disposable, Medical), a Class I device regulated under 21 CFR 880.6060.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 2, 1993
- Date Received
- May 26, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bedding, Disposable, Medical
- Device Class
- Class I
- Regulation Number
- 880.6060
- Review Panel
- HO
- Submission Type