510(k) K770509
- Device
- TABLE, MASSAGE AND TREATMENT
- Applicant
- Will Ross Co.
- 510(k) number
- K770509
- Product code
- INT
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-04-05
- Date received
- 1977-03-17
- Regulation
- 890.3520
- Classification name
- Plinth
- Medical specialty
- Physical Medicine
- Review panel
- Physical Medicine
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 2950684
- 1717548
- 2242467
- 3003947878
- 3007583774
- 3017264244
- 3030488262
- 3005004021
- 3008956940
Source Documents#
510(k) summary PDF not indicated by FDA