510(k) K911749
- Device
- L-linex-ray Fluorescence
- Applicant
- MONTIFORE MEDICAL CENTER
- 510(k) number
- K911749
- Product code
- JAO
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1991-08-20
- Date received
- 1991-04-18
- Regulation
- 892.1220
- Classification name
- Scanner, Fluorescent
- Medical specialty
- Radiology
- Review panel
- Radiology
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- JOHN F.ROSEN
- Address
- 111 E 210th St. Bronx NY US 10467 10467
Source Documents#
Other 510(k) Records For Product Code JAO#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K900574 | ABIOMED BODY LEAD ANALYZER MODEL 200/20 | Abiomed, Inc. | 1990-03-15 |