510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN

Cordis Webster, Inc.

Baldwin Park, CA, US

Cordis Webster, Inc. appears in FDA device records in Baldwin Park, CA. FDA records list 10 510(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
10
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 10 510(k) clearances for Cordis Webster, Inc. between 1995 and 1999. The busiest year on record is 1998, with 3. The most recent is 1999, with 2.

Clearances by year, as a table
510(k) clearance decisions for Cordis Webster, Inc., by decision year
YearClearances
19952
19962
19971
19983
19992
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K992965CORDIS WEBSTER FIXED CURVE CATHETERS, MODELS D-1124, D-1085DRFSubstantially Equivalent
K991531CORDIS WEBSTER DIAGNOSTIC DEFLECTABLE TIP CATHETER, MODEL D-1078DRFSubstantially Equivalent
K982740CORDIS WEBSTER PREFACE BRAIDED GUIDING SHEATH & PERRY EXCHANGE DILATOR, MODEL #'S 301-803A, 301-803P, 301-803M, 301-813SDYBSubstantially Equivalent
K982415CORDIS WEBSTER REF-STAR EXTERNAL REFERENCE PATCH, MODEL # D-1210DRFSubstantially Equivalent
K980961CORDIS WEBSTER REF-STAR EX SURFACE REFERENCE DEVICE MODEL'S D-1204-01, -02,-03, AND -04.DRFSubstantially Equivalent
K970264CORDIS WEBSTER BRAIDED GUIDING SHEATH EXCHANGE SYSTEMDYBSubstantially Equivalent
K953663CORDIS WEBSTER T20 DIAGNOSTIC DEFLECTABLE TIP CATHETERDRFSubstantially Equivalent
K955817CORIDIS WEBSTER DEFLECTABLE BRAIDED-TIP ELECTRODE CATHETERDRFSubstantially Equivalent
K954390CORDIS WESTER STAR CATHETERDRFSubstantially Equivalent
K953768CORDIS WEBSTER A20 DIAGNOSTIC DEFLECTABLE TIP CATHETERDRFSubstantially 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.

What MDM checks, and what it does not

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 Cordis Webster, Inc. 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 Cordis Webster, Inc.. 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