The following data is part of a premarket notification filed by Pentax Precision Instrument Corp. with the FDA for Eg-3630ur, Ultrasund Video Gastroscope.
Device ID | K013640 |
510k Number | K013640 |
Device Name: | EG-3630UR, ULTRASUND VIDEO GASTROSCOPE |
Classification | Gastroscope And Accessories, Flexible/rigid |
Applicant | PENTAX PRECISION INSTRUMENT CORP. 30 RAMLAND RD. Orangeburg, NY 10962 |
Contact | Paul Silva |
Correspondent | Paul Silva PENTAX PRECISION INSTRUMENT CORP. 30 RAMLAND RD. Orangeburg, NY 10962 |
Product Code | FDS |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-11-05 |
Decision Date | 2002-02-04 |
Summary: | summary |