510(k) K802884
- Device
- CORNING NORMAL GLYCOSYLATED HEMOGLOBIN
- Applicant
- CORNING MEDICAL & SCIENTIFIC
- 510(k) number
- K802884
- Product code
- JBD
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1980-12-22
- Date received
- 1980-11-17
- Regulation
- 864.7440
- Classification name
- System, Analysis, Electrophoretic Hemoglobin
- Medical specialty
- Hematology
- Review panel
- Hematology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 1618982
- 8023024
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code JBD #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K053571 | MICROGEL ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM, MICROGEL ACID HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM | Interlab S.R.L. | 2006-06-30 |
| K032862 | INTERLAB ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM | Interlab S.R.L. | 2004-02-03 |
| K992199 | ACID HEMOGLOBIN KIT | Helena Laboratories | 1999-09-21 |
| K991362 | HYDRAGEL HEMOGLOBIN(E), MINI HEMOGLOBIN(E), 7 HEMOGLOBIN(E), 15 HEMOGLOBIN(E), ACID(E) HEMOGLOBIN(E), MINI ACID(E) HEMO) | Morax | 1999-06-21 |
| K982426 | SPIFE ALKALINE HEMOGLOBIN | Helena Laboratories | 1998-12-17 |
| K931503 | REP HEMOGLOBIN IEF KITS (CAT. NO. 3250) | Helena Laboratories | 1993-08-16 |
| K931465 | REP ALKALINE HB-15 #3196,-8 #3197,-4 3198 | Helena Laboratories | 1993-07-06 |
| K901143 | REP HEMOGLOBIN IEF KITS (CAT. NO. 3250) | Helena Laboratories | 1990-05-23 |
| K830804 | LABILE REMOVING HEMOLYZING REAGENT | Corning Medical & Scientific | 1983-05-04 |
| K820518 | GELMAN GLYCO-PHORE BUFFER | Gelman Sciences, Inc. | 1982-04-09 |
| K813395 | CELLULOSE ACETATE-CITRATE AGAR HEMOGLO | Helena Laboratories | 1981-12-31 |
| K810919 | HEMOGLOBIN ELECTROPHORESIS CONTROL | Isolab, Inc. | 1981-04-23 |
| K810047 | AUTOPHOR 128 | Gelman Sciences, Inc. | 1981-02-05 |
| K802821 | PARAGON HEMOGLOBIN ELECTRO. REAG. KIT | Beckman Instruments, Inc. | 1980-12-11 |
| K800853 | A,SA2 LYOPHILIZED HEMO CONTROL | Helena Laboratories | 1980-04-29 |
Legacy Summary#
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FDA Review#
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