Preemicare Corp.
Houston, TX, US
Preemicare Corp. appears in FDA device records in Houston, TX. FDA records list 9 510(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
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Preemicare Corp. between 1988 and 1991. The busiest year on record is 1989, with 4. The most recent is 1991, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 1 |
| 1989 | 4 |
| 1990 | 3 |
| 1991 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K911450 | INFANT VENTILATOR | CBK | Substantially Equivalent | |
| K896375 | PREEMICARE NEBUTECH NEBULIZER SYSTEM | CAF | Substantially Equivalent | |
| K900735 | MODEL 130 AUTOMATIC HEIGHT ADJUST (AHA) INCUBATOR | FMZ | Substantially Equivalent | |
| K893622 | PREEMICARE MODEL 200-II INFANT TRANSPORT VENTIL. | CBK | Substantially Equivalent | |
| K893624 | PREEMICARE MODEL 2500 TRANSPORT WARMER | FPL | Substantially Equivalent | |
| K891674 | NEONATAL ENVIRONMENTAL MONITOR, MODEL 275 | CCL | Substantially Equivalent | |
| K885350 | PREEMICARE SERIES 2000 INFANT WARMER | FMT | Substantially Equivalent | |
| K884133 | PREEMICARE SERIES 4000 PHOTOTHERAPY LAMP | LBI | Substantially Equivalent | |
| K881476 | PREEMICARE MODEL D1-X1, SERIES 3000 | FMZ | 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