510(k) K812482

Device: FOAM WEDGE
Applicant: Maddak, Inc.
510(k) number: K812482
Product code: LDQ
Decision: Substantially Equivalent (SESE)
Decision date: 1981-09-24
Date received: 1981-08-31
Review panel: General Hospital
Clearance type: Traditional
Third party reviewed: No

Applicant Contact#

Address: 4221 Richmond Rd., NW Walker MI US 49534 49534

FDA Registration Numbers#

3004111573
1423537
1125615
3008061617
9612030
1061124
3004167615
9610849
9611024
9616088

Source Documents#

510(k) summary PDF not indicated by FDA