Martin Medical
Desoto, KS, US
Martin Medical appears in FDA device records in Desoto, KS. FDA records list 14 510(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
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Martin Medical between 1986 and 1987. The busiest year on record is 1987, with 8. The most recent is 1987, with 8.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1986 | 6 |
| 1987 | 8 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K873723 | PLASTER VACUUM, 230V MODEL NO. 4183-161 | LGH | Substantially Equivalent | |
| K873721 | PLASTER VACUUM, 115V MODEL NO. 4183-160 | LGH | Substantially Equivalent | |
| K873722 | PEDESTAL WALKING HEEL PRODUCT NO. 4183-133 | LGF | Substantially Equivalent | |
| K873720 | CAST CUTTER, 230V MODEL NO. 4183-107 | LGH | Substantially Equivalent | |
| K873719 | CAST CUTTER, 115V MODEL NO. 4183-106 | LGH | Substantially Equivalent | |
| K873718 | CHILD WALKING HEEL PRODUCT NO. 4183-132 | LGF | Substantially Equivalent | |
| K873717 | CUSHION TREAD WALKING HEEL PRODUCT NO. 4183-135 | LGF | Substantially Equivalent | |
| K873716 | ADULT WALKING HEEL PRODUCT NO. 4183-130 | LDF | Substantially Equivalent | |
| K863273 | MARTIN MEDICAL PRO-SCOPE ANOSCOPE | KOA | Substantially Equivalent | |
| K863275 | MARTIN MEDICAL PRO-SPEC SMALL VAGINAL SPECULUM | HIB | Substantially Equivalent | |
| K863274 | MARTIN MEDICAL PRO-SPEC MEDIUM VAGINAL SPECULUM | HIB | Substantially Equivalent | |
| K861075 | AMERICAN ORTHOPAEDIC CAST CUTTER, MODEL 0295-202 | LGF | Substantially Equivalent | |
| K861074 | AMERICAN ORTHOPAEDIC CAST CUTTER, MODEL 0295-200 | LGF | Substantially Equivalent | |
| K861073 | AMERICAN ORTHOPAEDIC VACUUM 0295-250 | LGF | 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