510(k) K770723

TABLE, TREATMENT, THERAPY, PHYSICAL by Chattanooga Pharmacal Co. — Product Code INT

K770723 is an FDA 510(k) premarket notification submitted by Chattanooga Pharmacal Co. for the device "TABLE, TREATMENT, THERAPY, PHYSICAL". The FDA issued a decision of Substantially Equivalent on July 11, 1977. The device falls under product code INT (Plinth), a Class I device regulated under 21 CFR 890.3520. Chattanooga Pharmacal Co. has at least 1 other 510(k) clearance on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 11, 1977
Date Received
April 19, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plinth
Device Class
Class I
Regulation Number
890.3520
Review Panel
PM
Submission Type