Atomic Products Corp.
Mchenry, IL, US
Atomic Products 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 Atomic Products Corp. between 1979 and 1992. The busiest year on record is 1990, with 4. The most recent is 1992, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1988 | 2 |
| 1989 | 1 |
| 1990 | 4 |
| 1991 | 1 |
| 1992 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K915541 | SPECT TABLE, MODEL #056-760 | IYZ | Substantially Equivalent | |
| K913055 | THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900 | IZD | Substantially Equivalent | |
| K904187 | ECONOMY C-ARM TABLE, MODEL # 056-005 | IXQ | Substantially Equivalent | |
| K904623 | RADIOGRAPHIC TRANSPORT, TRAUMA MODEL 056-230, 235 | IXQ | Substantially Equivalent | |
| K900851 | DIGITAL IMAGE ENHANCEMENT SYSTEM | LLZ | Substantially Equivalent | |
| K895799 | RECTILINEAR SCANNER MODEL #187-270 | IYW | Substantially Equivalent | |
| K884312 | ATOMLAB 100, MODEL 086-250 & 200 MODEL 086-270 | KPT | Substantially Equivalent | |
| K871868 | VENTI-SCAN II | IYT | Substantially Equivalent | |
| K874332 | MRI STRETCHER | FPO | Substantially Equivalent | |
| K790835 | DYNAJECT | DXT | 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
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Data as of , FDA export datePage updated Source: openFDA, public domain