FDA 510(k) Applications Submitted by ASAP ENDOSCOPIC PRODUCTS GMBH
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K121261 |
04/26/2012 |
ASAP MUITISCOPE |
ASAP ENDOSCOPIC PRODUCTS GMBH |
| K032822 |
09/10/2003 |
ASAP SINUSCOPE 10-0036-00,10-0037-00,10-0038,10-0039-00,10-0040-00,10-0041-00,10-0042-00,10-0043-00,10-0044-00,10-0045-0 |
ASAP ENDOSCOPIC PRODUCTS GMBH |
| K031141 |
04/10/2003 |
ASAP CYSTOSCOPE; ASAP LAPAROSCOPE; ASAP LARYGOSCOPE; ASAP OESOPHAGOSCOPE |
ASAP ENDOSCOPIC PRODUCTS GMBH |
| K031972 |
06/26/2003 |
ASAP ARTHROSCOPE MODELS; 10-0001-00, 10-0002-00, 10-0003-00, 10-0004-00, 10-0005-00, 10-0006-00, 10-0007-00, 10-0008-00, |
ASAP ENDOSCOPIC PRODUCTS GMBH |
| K031974 |
06/26/2003 |
ASAP HYSTEROSCOPE AND GYNECOLOGIC LAPAROSCOPE (SURGERY) 10-00018-00, 10-0019-00, 100020-00, 10-0021-00, 10-0022-00, 10-0 |
ASAP ENDOSCOPIC PRODUCTS GMBH |
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