Bailey Mfg. Co.
Lodi, OH, US
Bailey Mfg. Co. appears in FDA device records in Lodi, OH. 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 Bailey Mfg. Co. between 1993 and 1994. The busiest year on record is 1993, with 10. The most recent is 1994, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1993 | 10 |
| 1994 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K932240 | MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS | IRR | Substantially Equivalent | |
| K932241 | ECONOMY HI-LOW MAT TABLES/ELECTRIC MODELS | INQ | Substantially Equivalent | |
| K932239 | ELECTRIC TILT TABLE MODEL 9505 | INQ | Substantially Equivalent | |
| K932238 | ECO. HI-LOW TREATMENT TABLES VARIOUS MODEL NUMBERS | INW | Substantially Equivalent | |
| K932237 | PRO. HI-LOW TREATMENT TABLES MODELS 4050,4070,4090 | INQ | Substantially Equivalent | |
| K932236 | PRO. HI-LOW TABLE MODEL 9530 | INQ | Substantially Equivalent | |
| K932235 | PRO. HI-LOW MAT TABLES #9610-9612 9620-9622 | INQ | Substantially Equivalent | |
| K932234 | PROFESSIONAL & ECONMY TILT TABLE 9500 9520 | INW | Substantially Equivalent | |
| K932233 | ECONOMY HI-LOW WORK TABLE (MANUAL) MODEL 3405 | INW | Substantially Equivalent | |
| K932232 | PROFESSONAL HI-LOW WORK TABLE MODEL 3400 | INQ | Substantially Equivalent | |
| K932231 | ECONOMY HI-LOW MAT TABLE #4110 THRU 4117 | INW | 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
