510(k) K802829

SCANLAN VASCU-STATT by Scanlan Intl., Inc. — Product Code FMP

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