510(k) K851719
- Device
- 1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS
- Applicant
- ARTIBERIA
- 510(k) number
- K851719
- Product code
- EZZ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1985-07-02
- Date received
- 1985-04-25
- Regulation
- 510(k) Premarket Notification
- Classification name
- Prosthesis, Vas Deferens
- Medical specialty
- 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
- Review panel
- Gastroenterology/Urology
- Device class
- 3
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- GIL M SANCHEZ
- Address
- 4518 Los Ranchitos San Antonio TX US 78233 78233
Source Documents#
510(k) summary PDF not indicated by FDA
Legacy Summary#
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FDA Review#
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