510(k) K770632
- Device
- GAS COLLHCTOR BE 155(155-2-3,154-4)
- Applicant
- Instrumentation Industries, Inc.
- 510(k) number
- K770632
- Product code
- KGK
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-04-08
- Date received
- 1977-04-04
- Regulation
- 868.1575
- Classification name
- Gas, Collecting Vessel
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- 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#
- 8043316
- 3006783791
- 3010223399
- 3004852415
- 2080783
- 3032133057
- 3014146451
- 9611252
- 3016852448
- 3013501110
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code KGK#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K863171 | RESPIRONICS PROTECTEASY | Respironics, Inc. | 1986-10-15 |