Peripheral Systems Group
Mountain View, CA, US
Peripheral Systems Group appears in FDA device records in Mountain View, CA. FDA records list 17 510(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
- 17
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 17 510(k) clearances for Peripheral Systems Group between 1990 and 1994. The busiest year on record is 1990, with 6. The most recent is 1994, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1990 | 6 |
| 1991 | 3 |
| 1992 | 3 |
| 1993 | 4 |
| 1994 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K940804 | SMARTNEEDLE VASCULAR ACCESS SYSTEM, MODIFICATION | ITX | Substantially Equivalent | |
| K934433 | VANTAGE DIALTAION CATHETER | LIT | Substantially Equivalent | |
| K932777 | SMARTNEEDLE(R) OVER-THE-NEEDLE CATHETER | ITX | Substantially Equivalent | |
| K931327 | PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE | DQX | Substantially Equivalent | |
| K915554 | HI-TORQUE SPORT-T(TM) GUIDE WIRE | DQX | Substantially Equivalent | |
| K914979 | EDM(R) INFUSION CATHETER | KRA | Substantially Equivalent | |
| K913941 | PSG(TM) 20 GUAGE DOPPLER NEEDLE | ITX | Substantially Equivalent | |
| K915168 | PROFLEX 5 | LIT | Substantially Equivalent | |
| K913477 | APEX(TM) PROSTATIC BALLOON DILATION CATHETER | KOE | Substantially Equivalent | |
| K913746 | SMARTNEEDLE(TM) VASCULAR ACCESS SYSTEM | ITX | Substantially Equivalent | |
| K904984 | ADVANCE 418(TM) | LIT | Substantially Equivalent | |
| K904959 | PSG HEMOSTATIC CONTROL VALVE | DQO | Substantially Equivalent | |
| K903625 | DOPPLER NEEDLE AND FLOW MONITOR | DPW | Substantially Equivalent | |
| K895179 | ACCESSOR PERIPHERAL DILATING GUIDE WIRE | LIT | Substantially Equivalent | |
| K895146 | GUIDING CATHETER | DQO | Substantially Equivalent | |
| K894944 | BALLOON DILATATION CATHETER | LIT | Substantially Equivalent | |
| K895932 | PSG(TM) EDM(TM) INFUSION CATHETER | DQY | 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
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.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Peripheral Systems Group edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
The self-serve claim needs an FDA establishment registration, FEI or owner-operator number on the company’s record, and we hold none for Peripheral Systems Group. The only route for a company with no identifier on record is a person here: write to us, and one looks at the record and sends the same claim link by hand.
Data as of , FDA export datePage updated Source: openFDA, public domain