Minnetonka, Inc.
Walker, MI, US
Minnetonka, Inc. appears in FDA device records in Walker, MI. FDA records list 4 510(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
- 4
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 4 510(k) clearances for Minnetonka, Inc. between 1983 and 1989. The busiest year on record is 1989, with 2. The most recent is 1989, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 1 |
| 1986 | 1 |
| 1989 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K883619 | MEDICATED COVERING COATED W/1.0% HYDRO ADHES. GEL | SEK | Substantially Equivalent for Some Indications | |
| K883566 | MEDICATED COVERING COATED W/.5% HYDRO ADHESIVE GEL | SEK | Substantially Equivalent for Some Indications | |
| K860843 | CHECK-UP PLAQUE FIGHTING GUM | EJR | Substantially Equivalent | |
| K831488 | DAVRON PROF. SCRUB BRUSH-DRY/STERILE | GEC | 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