510(k) K904761
- Device
- P/n 35310, Il Test Alkaline Phosphatase Reagent
- Applicant
- INSTRUMENTATION LABORATORY CO.
- 510(k) number
- K904761
- Product code
- CIE
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1990-11-20
- Date received
- 1990-10-19
- Regulation
- 862.1160
- Classification name
- Volumetric/Manometric, Carbon-Dioxide
- Medical specialty
- Clinical Chemistry
- Review panel
- Clinical Chemistry
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- GEORGE A LYNA
- Address
- 113 Hartwell Ave. P.O. Box 9113 Lexington MA US 02173 02173
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code CIE#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K880967 | MICRO CO2 APPARATUS | Hf Scientific, Inc. | 1988-04-28 |
| K864313 | CO2 REAGENT SET | Hf Scientific, Inc. | 1987-03-13 |
| K832071 | TOTAL CO2 REAGENT SET | American Research Products Co. | 1983-08-11 |
| K820091 | AIRMED SMOKE EVACUATION & FILTER | James L. Geraci & Associates, Inc. | 1982-02-24 |
| K800524 | SERALYZER REFLECTANCE PHOTOMETER/CALIB. | Miles Laboratories, Inc. | 1980-04-02 |
| K771610 | CARBON DIOXIDE ANALYZER | Corning Medical & Scientific | 1977-10-07 |