Vitaphore Corp.
San Francisco, CA, US
Vitaphore Corp. appears in FDA device records in San Francisco, CA. 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 Vitaphore Corp. between 1986 and 1992. The busiest year on record is 1990, with 5. The most recent is 1992, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1986 | 1 |
| 1987 | 1 |
| 1988 | 2 |
| 1989 | 1 |
| 1990 | 5 |
| 1991 | 2 |
| 1992 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K914579 | SILVER FOAM WOUND DRESSING | FRO | Substantially Equivalent | |
| K913148 | COLLAGEN SHIELD FOR ACUTE CARE | MOE | Substantially Equivalent | |
| K895920 | VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS | KGX | Substantially Equivalent | |
| K902558 | COLLAGEN SHIELD FOR ACUTE CARE | MOE | Substantially Equivalent | |
| K891993 | COLLAGEN NEUROSPONGE | HBA | Substantially Equivalent | |
| K896455 | VITACHOICE WOUND DRESSING | KGX | Substantially Equivalent | |
| K896046 | VITAPATCH CATH. SECUREMENT DEVICE W/CHLORHEXIDINE | KMK | Substantially Equivalent | |
| K895993 | VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE | KMK | Substantially Equivalent | |
| K890435 | VITAACCESS CATHETER INTRODUCER KIT | FOZ | Unknown | |
| K882100 | VITACUFF(R) PERCUTANEOUS INFECT. CONTROL KIT | LJS | Substantially Equivalent | |
| K872998 | VITAACCESS (TM) CATHETER INTRODUCER SYSTEM | FOZ | Substantially Equivalent | |
| K872538 | VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS | JEC | Substantially Equivalent | |
| K861563 | VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT | LJS | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- MOECollagen Corneal Shield
- JECComponent, Traction, Invasive
- KMKDevice, Intravascular Catheter Securement
- FRODressing, Wound, Drug
- HBANeurosurgical Paddie
- KGXTape And Bandage, Adhesive
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain