510(k) K023690
- Device
- CATHETER CONNECTOR
- Applicant
- WORLD METALS, INC,
- 510(k) number
- K023690
- Product code
- KNY
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2003-02-28
- Date received
- 2002-11-01
- Regulation
- 876.5130
- Classification name
- Accessories, Catheter, G-u
- Medical specialty
- Gastroenterology/Urology
- Review panel
- Gastroenterology/Urology
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
- Source
- FDA openFDA 510(k) dataset plus migrated FDA.report data
Related Records
Applicant Contact
- Contact
- MARTIN MITCHELL
- Address
- 1020 NE 27 Ave. Pompano Beach FL US 33062 33062
FDA Registration Numbers
- 3002807314
- 9680787
- 3012322232
- 3004111573
- 1018233
- 9681477
- 3009763019
- 9612030
- 3003790304
- 3006174295
- 8010418
- 1625425
- 9611590
- 2183744
- 1921846
- 2032098
- 3005232773
- 3010155661
- 2020550
- 3003915875
- 2032112
- 3016096097
- 3006082230
- 3011050570
- 1713468
- 2029015
- 9617594
- 3010202439
- 9610617
- 2022435
- 1423537
- 3014342096
- 2027111
- 3016171914
- 3010707607
- 2029275
- 3009051888
- 2126666
Source Documents
FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON
Legacy Summary
summary
FDA Review
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