Medi-Flex Hospital Products, Inc.
Overland Park, KS, US
Medi-Flex Hospital Products, Inc. appears in FDA device records in Overland Park, KS. FDA records list 13 510(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
- 13
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 13 510(k) clearances for Medi-Flex Hospital Products, Inc. between 1991 and 1997. The busiest year on record is 1995, with 4. The most recent is 1997, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1991 | 1 |
| 1992 | 1 |
| 1993 | 2 |
| 1994 | 3 |
| 1995 | 4 |
| 1996 | 1 |
| 1997 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K970441 | K-KLOSURE 2 INCH LENGTH/4 INCH LENGTH/8 INCH LENGTH/12 INCH LENGTH | FPX | Substantially Equivalent | |
| K962740 | DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641 | KMF | Substantially Equivalent | |
| K952201 | PORT-A-CATH ACCESS KIT | FMF | Substantially Equivalent | |
| K952416 | TRACHEOSTOMY CARE KIT | BTO | Unknown | |
| K952256 | PICC LINE KIT | FOZ | Substantially Equivalent | |
| K952007 | ADHEROL SEPP APPLICATOR | FRO | Substantially Equivalent | |
| K934790 | SEPP ADHESIVE REMOVER | KOX | Substantially Equivalent | |
| K923516 | COMPOUND BENZOIN TINCTURE USP SEPP | KMF | Substantially Equivalent | |
| K920399 | COMPOUND BENZOIN TINCTURE USP FREPP | KMF | Substantially Equivalent | |
| K930196 | CEPTI-SEAL I.V. PREP KIT | LRS | Unknown | |
| K921347 | CEPTI-SEAL DRESSING CHANGE KIT FOR VENOUS CATHETER | MCY | Unknown | |
| K920398 | CEPTI-SEAL DRESSING CHNG. KIT FOR CENT. VENOUS CAT | FMF | Substantially Equivalent | |
| K914316 | CEPTI-SEAL DRESSING CHANGE KIT FOR CENT VEN CATH | LYY | Substantially Equivalent for Some Indications |
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