510(k) K781330
- Device
- Blood Level Detector-model 7601
- Applicant
- BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
- 510(k) number
- K781330
- Product code
- FJF
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1978-08-31
- Date received
- 1978-08-02
- Regulation
- 876.5820
- Classification name
- Detector, Air Bubble
- Medical specialty
- Gastroenterology, Urology
- Review panel
- Gastroenterology, Urology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 1875 Eye St. NW Suite 625 Washington DC US 20006 20006
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FJF#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K904992 | MINNILERT AIR DETECTOR | Minntech Corp. | 1991-02-05 |
| K891327 | NICKLE-TITANIUM ORTHODONTIC WIRE | American Orthodontics | 1989-05-10 |
| K780582 | DETECTOR, BUBBLE & FOAM | Hospal Medical Corp. | 1978-06-22 |
| K770857 | DIALYSIS MACHINE, CENTRY II | Cobe Laboratories, Inc. | 1977-10-04 |