510(k) K790057
- Device
- Catheter, Oxygen
- Applicant
- MEDLINE INDUSTRIES, INC.
- 510(k) number
- K790057
- Product code
- BZB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1979-02-05
- Date received
- 1979-01-09
- Regulation
- 868.5350
- Classification name
- Catheter, Nasal, Oxygen
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- 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#
- 3014810929
- 3015173212
- 3016763307
- 3043619925
- 3014437893
- 9613418
- 3011987967
- 3029706818
- 1836161
- 3013440654
- 3017406698
- 3016734145
- 3039440874
- 3007092328
- 1417592
- 3008808560
- 3010621964
- 3015058854
- 3006210673
- 3003882387
- 3008806809
- 3012002722
- 9613910
- 3007649127
- 3010131137
- 8030673
- 3014632157
- 3016426851
- 1924066
- 9616083
- 3005273623
- 1314417
- 3002808270
- 3003965134
- 3004122598
- 3013846070
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code BZB#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K896731 | OXYGEN CATHETERS | Unoplast A/S | 1990-03-30 |
| K843466 | PHARMA-PLAST OXYGEN CATHETER | Zimmar Consulting , Ltd. | 1984-11-19 |
| K833351 | DEMAND OXYGEN CONTROLLER | Healthdyne, Inc. | 1984-03-19 |
| K830984 | OXYGEN CATHETERS | Medovations, Inc. | 1983-05-18 |
| K820370 | NASAL OXYGEN CATHETER | American Pharmaseal Div. Ahsc | 1982-04-16 |
| K800506 | OXYGEN CATHETER | Medi-Craft , Ltd. | 1980-03-25 |
| K791273 | CONPHAR OXYGEN CATHETER-STERILE | Conphar, Inc. | 1979-07-24 |