Company ยท US
Vitaphore Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 1992. Name variants (Inc, Corp, punctuation) are merged.
13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | 2 |
| KGX | Tape And Bandage, Adhesive | 2 |
| KMK | Device, Intravascular Catheter Securement | 2 |
| LJS | Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days | 2 |
| MOE | Collagen Corneal Shield | 2 |
| FRO | Dressing, Wound, Drug | 1 |
| HBA | Neurosurgical Paddie | 1 |
| JEC | Component, Traction, Invasive | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Feb 21, 1992 | K914579 | SILVER FOAM WOUND DRESSING Vitaphore Corp. | FRO |
| Oct 15, 1991 | K913148 | COLLAGEN SHIELD FOR ACUTE CARE Vitaphore Corp. | MOE |
| Jun 6, 1991 | K895920 | VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS Vitaphore Corp. | KGX |
| Aug 17, 1990 | K902558 | COLLAGEN SHIELD FOR ACUTE CARE Vitaphore Corp. | MOE |
| Mar 23, 1990 | K891993 | COLLAGEN NEUROSPONGE Vitaphore Corp. | HBA |
| Feb 15, 1990 | K896455 | VITACHOICE WOUND DRESSING Vitaphore Corp. | KGX |
| Jan 11, 1990 | K896046 | VITAPATCH CATH. SECUREMENT DEVICE W/CHLORHEXIDINE Vitaphore Corp. | KMK |
| Jan 11, 1990 | K895993 | VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE Vitaphore Corp. | KMK |
| Mar 29, 1989 | K890435 | VITAACCESS CATHETER INTRODUCER KIT Vitaphore Corp. | FOZ |
| Jul 13, 1988 | K882100 | VITACUFF(R) PERCUTANEOUS INFECT. CONTROL KIT Vitaphore Corp. | LJS |
| Mar 24, 1988 | K872998 | VITAACCESS (TM) CATHETER INTRODUCER SYSTEM Vitaphore Corp. | FOZ |
| Jul 10, 1987 | K872538 | VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS Vitaphore Corp. | JEC |
| Aug 27, 1986 | K861563 | VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT Vitaphore Corp. | LJS |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||