510(k) K770611
- Device
- PARALLEL BARS
- Applicant
- Will Ross Co.
- 510(k) number
- K770611
- Product code
- IOE
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-04-08
- Date received
- 1977-03-31
- Regulation
- 890.5370
- Classification name
- Bars, Parallel, Exercise
- 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#
- 3006123327
- 2242467
- 3015142701
- 3012251300
- 3038636181
- 3007278668
- 1649977
- 3014270896
- 3007218972
- 3017264244
- 9614093
- 3001452523
- 3004499949
- 3008309560
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code IOE#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K830466 | BARS, PARALLEL, EXERCISE | Kaye Products, Inc. | 1983-03-09 |