Supelco, Inc.
Mchenry, IL, US
Supelco, Inc. appears in FDA device records in Mchenry, IL. FDA records list 24 510(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
- 24
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 24 510(k) clearances for Supelco, Inc. between 1976 and 1989. The busiest year on record is 1988, with 6. The most recent is 1989, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 1 |
| 1977 | 1 |
| 1980 | 3 |
| 1981 | 4 |
| 1982 | 1 |
| 1984 | 3 |
| 1986 | 3 |
| 1987 | 1 |
| 1988 | 6 |
| 1989 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K894141 | LIQUID CHROMATOGRAPHY COLUMNS | DPM | Substantially Equivalent | |
| K884403 | LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBE | DPM | Substantially Equivalent | |
| K883615 | LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73 | DJY | Substantially Equivalent | |
| K881868 | LIQUID CHROMATOGRAPHY COLUMNS HISEP COLUMN & GUARD | DPM | Substantially Equivalent | |
| K881361 | SOLID PHASE EXTRACTION TUBES | DJY | Substantially Equivalent | |
| K880724 | LIQUID CHROMATO. COLUMNS | DPM | Substantially Equivalent | |
| K874824 | CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY | DII | Substantially Equivalent | |
| K871174 | 4-9295 BARBITURATES TEST MIX | DKB | Substantially Equivalent | |
| K862542 | CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY | DII | Substantially Equivalent | |
| K862541 | LIQUID CHROMATOGRAPHY COLUMNS | DPM | Substantially Equivalent | |
| K861633 | LIQUID CHROMATOGRAPHY COLUMNS | DPM | Substantially Equivalent | |
| K842909 | LIQUID CHROMATOGRAPHY COLUMNS;ION EXCH | DPM | Substantially Equivalent | |
| K841712 | CAPILLARY GAS CHROMATOGRAPHIC COLUMNS | DII | Substantially Equivalent | |
| K833276 | DRUG STANDARDS | DKB | Substantially Equivalent | |
| K813575 | LIQUID CHROMATOGRAPHY (HPLC) COLUMNS | DPM | Substantially Equivalent | |
| K811674 | DRUG STANDARDS | DKB | Substantially Equivalent | |
| K811304 | LIQUID CHROMATOGRAPHY COLUMNS | DPM | Substantially Equivalent | |
| K810743 | LECITHIN-SPINGOMYELIN STAND. & KITS | JIS | Substantially Equivalent | |
| K810742 | AQUEOUS TRIOLEIN STANDARDS & KITS | JIS | Substantially Equivalent | |
| K802278 | IN VITRO DIAGNOSTIC STANDARDS | DIF | Substantially Equivalent | |
| K802703 | LIQUID CHROMATOGRAPHY COLUMNS | DPM | Substantially Equivalent | |
| K801833 | GAS-CHROMATOGRAPHIC PACKING | DJA | Substantially Equivalent | |
| K761226 | GP3%SP-2100DOHON100/120 MESH SUPELCOPORT | JSQ | Substantially Equivalent | |
| K761156 | AMINOGLYCOSIDE CONTROLS | DAS | 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.
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Data as of , FDA export datePage updated Source: openFDA, public domain