510(k) K801628

RESTRAINT, PROTECTIVE by The Owenby Co. — Product Code IQK

K801628 is an FDA 510(k) premarket notification submitted by The Owenby Co. for the device "RESTRAINT, PROTECTIVE". The FDA issued a decision of Substantially Equivalent on August 7, 1980. The device falls under product code IQK (Orthosis, Cervical), a Class I device regulated under 21 CFR 890.3490. The Owenby Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 7, 1980
Date Received
July 15, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Orthosis, Cervical
Device Class
Class I
Regulation Number
890.3490
Review Panel
PM
Submission Type