Dermacare Products, Inc.
Louisville, KT, US
Dermacare Products, Inc. appears in FDA device records in Louisville, KT. FDA records list 8 510(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
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Dermacare Products, Inc. between 1985 and 1988. The busiest year on record is 1986, with 4. The most recent is 1988, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 1 |
| 1986 | 4 |
| 1987 | 1 |
| 1988 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K882494 | ELAN-E DISPOSALBE DRAPE | KKX | Substantially Equivalent | |
| K882421 | INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE | JOS | Substantially Equivalent | |
| K871910 | SURGITEK DISPOSABLE BIPOLAR CORD | GEI | Substantially Equivalent | |
| K863280 | DERMAMARKER | FZZ | Substantially Equivalent | |
| K863279 | SURGI-TEK TUBE POSITIONER | Substantially Equivalent | ||
| K863278 | SURGI-WIPES | Substantially Equivalent | ||
| K862367 | PRO-CLEAN | Substantially Equivalent | ||
| K853374 | CORRECT-A-COUNT | 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