Electromek Diagnostic Systems, Inc.
Troy, IL, US
Electromek Diagnostic Systems, Inc. appears in FDA device records in Troy, IL. FDA records list 11 510(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
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Electromek Diagnostic Systems, Inc. between 1990 and 1991. The busiest year on record is 1990, with 10. The most recent is 1991, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1990 | 10 |
| 1991 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K902986 | G.E. DXD 325/350/350II/DXD 525/525II GENERATORS | IZO | Substantially Equivalent | |
| K902987 | G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORS | IZO | Substantially Equivalent | |
| K902988 | G.E. MSI 850/850II/1250 THREE PHASE GENERATORS | IZO | Substantially Equivalent | |
| K902985 | G.E. MST 625/625II/MST 1050/1050II THREE PHASE GEN | IZO | Substantially Equivalent | |
| K902982 | G.E. POLARIX II C-ARM | JAA | Substantially Equivalent | |
| K902981 | G.E. FLUOROCON 300 IMAGING SYSTEM | JAA | Substantially Equivalent | |
| K902983 | SIEMEN'S SIREMOBILE II C-ARM | JAA | Substantially Equivalent | |
| K902989 | G.E. MONITROL 90 AND G.E. MONITROL 15 | IXR | Substantially Equivalent | |
| K902791 | G.E. 48-4 CEILING TUBEHANGER | KPR | Substantially Equivalent | |
| K902984 | G.E. AMX 110, AMX II AND AMX 3 X-RAY UNITS | IZL | Substantially Equivalent | |
| K902980 | G.E. XT CEILING TUBE SUSPENSION | JAA | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
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 Electromek Diagnostic Systems, Inc. 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 Electromek Diagnostic Systems, Inc.. 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