FDA 510(k) Applications Submitted by JOHN MILLER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K072262 |
08/15/2007 |
GENTLERAY 980 DIODE LASER SYSTEM |
KAVO AMERICA |
| K964539 |
11/12/1996 |
PORTABLE SERIES REVERSE OSMOSIS SYSTEMS 700, 701, 702, 703, 704, 750, MRE-NF, F800-F802, RO SECURA, REVERSE OSMOSIS SYST |
ZYZATECH WATER SYSTEMS, INC. |
| K962805 |
07/18/1996 |
SPYGLASS ANGIOGRAPHIC CATHETER |
DAIG CORP. |
| K964518 |
10/25/1996 |
FAST-CATH TRANSSEPTAL CATHETER INTRODUCER |
DAIG CORP. |
| K965249 |
12/12/1996 |
SPYGLASS ANGIOGRAPHIC CATHETER |
DAIG CORP. |
| K050019 |
01/05/2005 |
IN EXAM INTRAORAL DENTAL X-RAY SYSTEM |
KAVO AMERICA |
| K050255 |
02/03/2005 |
ARTHORALIX 8500, MODELS 110-0199G1, 110-0199G2, 110-0199G3, 110-0199G4 |
GENDEX DENTAL SYSTEMS |
| K032355 |
07/30/2003 |
ORTHORALIX 9200 DDE, ORTHORALIX 9200 DDE PLUS CEPH, MODELS 5105 0161WW, 5105 0181WW |
DENTSPLY GENDEX |
| K032904 |
09/17/2003 |
ACUCAM CONCEPT IV FWT, MODEL 110-0185G1 |
DENTSPLY INTL. |
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