510(k) K780230

Device: Bed Board
Applicant: BIOMET, INC.
510(k) number: K780230
Product code: FPS
Decision: Substantially Equivalent (SESE)
Decision date: 1978-02-28
Date received: 1978-02-09
Regulation: 880.6070
Classification name: Board, Bed
Medical specialty: General Hospital
Review panel: General Hospital
Device class: 1
Clearance type: Traditional
Third party reviewed: No

Applicant Contact#

Address: 803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

3007307488
3017607477
3033849261
3008485769
3010030809
3009408502
8022890
1422443

Source Documents#

510(k) summary PDF not indicated by FDA