Hdc Corp.
San Jose, CA, US
Hdc Corp. appears in FDA device records in San Jose, CA. FDA records list 12 510(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
- 12
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 12 510(k) clearances for Hdc Corp. between 1992 and 2001. The busiest year on record is 1995, with 3. The most recent is 2001, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1992 | 1 |
| 1995 | 3 |
| 1996 | 1 |
| 1997 | 1 |
| 1998 | 2 |
| 1999 | 1 |
| 2000 | 2 |
| 2001 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K010425 | EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY) | KNF | Substantially Equivalent | |
| K994059 | CLA KIT (CONTINUOUS LOCAL ANESTHESIA), MODEL 551-17, 551-10, 551-07 | CAZ | Substantially Equivalent | |
| K002770 | IBIS CHEMO-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM, MODEL 700-08-10,700-08-11,700-08-12,700-08-15,700-08-16,735-08-10 | LJT | Substantially Equivalent | |
| K983119 | ENTERO-TEST HP, MODEL #102-01 | LIO | Substantially Equivalent | |
| K983916 | V-CATH PICC (PERIPHERALLY INSERTED CENTRAL CATHETER) | FOZ | Substantially Equivalent | |
| K983409 | V-CATH PICC (PERIPHERALLY INSERTED CENTRAL CATHETER) SEE APPENDIX 1 | FOZ | Substantially Equivalent | |
| K964966 | V-CATH | FOZ | Substantially Equivalent | |
| K953300 | V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER | LJS | Substantially Equivalent | |
| K951384 | V-CATH PERCUTANEOUS INTRODUCER KIT | KZH | Substantially Equivalent | |
| K951098 | HDC VADD (VASCULAR ACCESS DEVICE) TUNNELER | LJS | Substantially Equivalent | |
| K945473 | V-CATH BREAKAWAY NEEDLE INTRODUCER | KZH | Substantially Equivalent | |
| K913386 | CHEMO-PORT | FMI | Unknown |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- CAZAnesthesia Conduction Kit
- LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- KNFCoagulator-Cutter, Endoscopic, Unipolar (And Accessories)
- LIODevice, Specimen Collection
- KZHIntroducer, Syringe Needle
- FMINeedle, Hypodermic, Single Lumen
- LJTPort & Catheter, Implanted, Subcutaneous, Intravascular
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