Cambridge Medical Technology
Mchenry, IL, US
Cambridge Medical Technology appears in FDA device records in Mchenry, IL. FDA records list 14 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Cambridge Medical Technology between 1982 and 1989. The busiest year on record is 1984, with 3. The most recent is 1989, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 1 |
| 1983 | 1 |
| 1984 | 3 |
| 1985 | 1 |
| 1986 | 3 |
| 1987 | 2 |
| 1989 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K890837 | RIA-GNOST INSULIN | CFP | Substantially Equivalent | |
| K890836 | RIA-GNOST PROGESTERONE | JLS | Substantially Equivalent | |
| K890697 | RIA-GNOST FERRITIN | JMG | Substantially Equivalent | |
| K873737 | NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAY | CDP | Substantially Equivalent | |
| K870573 | T4 NO SPIN(TM) COATED TUBE RADIOIMMUNOASSAY KIT | CDX | Substantially Equivalent | |
| K862871 | RADIOIMMUNOASSAY OF NO SPIN(TM) CORTISOL | CGR | Substantially Equivalent | |
| K860130 | TESTOSTERONE COATED TUBES RADIOIMMUNOASSAY KIT | CDZ | Substantially Equivalent | |
| K855169 | T3 UPTAKE RADIOIMMUNOASSAY KIT | KHQ | Substantially Equivalent | |
| K850254 | PARATHYROID HORMONE RADIOIMMUNOASSAY KIT | CEW | Substantially Equivalent | |
| K843635 | MATCHED COMPONENT SET FOR RADIOIMMUNO- | JKC | Substantially Equivalent | |
| K841042 | MATCHED COMPONENT SET RADIOIMMUNOASSAY | CDZ | Substantially Equivalent | |
| K834080 | MATCHED COMPONENT SET FOR DIGITOXIN | LCW | Substantially Equivalent | |
| K830148 | CORTISOL KIT | CGR | Substantially Equivalent | |
| K821811 | 125I DIGOXIN RADIOIMMUNOASSAY KIT | DPB | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KHQRadioassay, Triiodothyronine Uptake
- JMGRadioimmunoassay (Two-Site Solid Phase), Ferritin
- CGRRadioimmunoassay, Cortisol
- JKCRadioimmunoassay, Dehydroepiandrosterone (Free And Sulfate)
- LCWRadioimmunoassay, Digitoxin (125-I)
- DPBRadioimmunoassay, Digoxin (125-I), Rabbit Antibody, Charcoal Sep.
- CFPRadioimmunoassay, Immunoreactive Insulin
- CEWRadioimmunoassay, Parathyroid Hormone
- JLSRadioimmunoassay, Progesterone
- CDZRadioimmunoassay, Testosterones And Dihydrotestosterone
- CDXRadioimmunoassay, Total Thyroxine
- CDPRadioimmunoassay, Total Triiodothyronine
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain