510(k) K802829
K802829 is an FDA 510(k) premarket notification submitted by Scanlan Intl., Inc. for the device "SCANLAN VASCU-STATT". The FDA issued a decision of Substantially Equivalent on January 15, 1981. The device falls under product code FMP (Protector, Skin Pressure), a Class I device regulated under 21 CFR 880.6450. Scanlan Intl., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 15, 1981
- Date Received
- November 10, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Protector, Skin Pressure
- Device Class
- Class I
- Regulation Number
- 880.6450
- Review Panel
- HO
- Submission Type