Damon Corp.
Mchenry, IL, US
Damon Corp. appears in FDA device records in Mchenry, IL. FDA records list 10 510(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
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for Damon Corp. between 1976 and 1983. The busiest year on record is 1977, with 2. The most recent is 1983, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 1 |
| 1977 | 2 |
| 1978 | 2 |
| 1979 | 2 |
| 1980 | 1 |
| 1982 | 1 |
| 1983 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K831826 | ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY | CKG | Substantially Equivalent | |
| K820686 | LIQUISOL PROGESTERONE RADIOIMMUNO | JLS | Substantially Equivalent | |
| K802661 | LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT | CDZ | Substantially Equivalent | |
| K790250 | LIQUISOL CORTISOL RIA TEST KIT | Substantially Equivalent | ||
| K782124 | IEC CENTRA-7 CENTRIFUGE MODEL 2362 | JQC | Substantially Equivalent | |
| K781012 | RIA TEST KIT SYS. DAMON KIQUISOL FREE | CEC | Substantially Equivalent | |
| K780207 | LIQUISOL DIGOXIN RIA TEST KIT | DON | Substantially Equivalent | |
| K770918 | LIQUI SOL T4 RIA TEST KIT | CDP | Substantially Equivalent | |
| K770606 | ANALYZEO, PLASMA, BLOOD, COLYSAGRAPH | JPA | Substantially Equivalent | |
| K761013 | SPINETTE CENTRIFUGE | JQC | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- JQCCentrifuges (Micro, Ultra, Refrigerated) For Clinical Use
- CKGRadioimmunoassay, Acth
- DONRadioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.
- CECRadioimmunoassay, Free Thyroxine
- JLSRadioimmunoassay, Progesterone
- CDZRadioimmunoassay, Testosterones And Dihydrotestosterone
- CDPRadioimmunoassay, Total Triiodothyronine
- JPASystem, Multipurpose For In Vitro Coagulation Studies
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.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Damon Corp. edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
The self-serve claim needs an FDA establishment registration, FEI or owner-operator number on the company’s record, and we hold none for Damon Corp.. The only route for a company with no identifier on record is a person here: write to us, and one looks at the record and sends the same claim link by hand.
Data as of , FDA export datePage updated Source: openFDA, public domain