510(k) K934496
- Device
- X-RAY ANGIOGRAPHIC SYSTEM
- Applicant
- CAMTRONICS, LTD.
- 510(k) number
- K934496
- Product code
- IZI
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1993-12-13
- Date received
- 1993-09-15
- Regulation
- 892.1600
- Classification name
- System, X-ray, Angiographic
- Medical specialty
- Radiology
- Review panel
- Radiology
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- ROBERT K RIEDERMANN
- Address
- Medical Systems 900 Walnut Ridge Dr., Box 950 Hartland WI US 53029 53029
FDA Registration Numbers#
- 3003755939
- 3015231789
- 3029968414
- 3004122598
- 3004977335
- 3004519921
- 1422634
- 3021336182
- 1048735
- 3042243691
- 3036666444
- 9611343
- 3018126215
- 3035950510
- 3012939903
- 3030926959
- 1000181430
- 3000976525
- 1625425
- 3010326005
- 1319639
- 3021059265
- 3012761544
- 3008284470
- 3033527282
- 2648727
- 3004026651
- 3014262693
- 3015276088
- 3006498370
- 3020746799
- 3012345110
- 1043214
- 1018470
- 3014004349
- 1000204638
- 3015532525
- 3045816907
- 3012329552
- 3013283620
- 3009963139
- 3006990600
- 3013764800
- 3021393544
- 3011416394
- 3005810333
- 2916714
- 3003768277
- 3023003446
- 3020704423
- 9613445
- 3007138831
- 1054241
- 3013700547
- 3014321789
- 1644312
- 3003202425
- 3009057691
- 3003637092
- 3022626486
- 3015806723
- 3020899789
- 9610612
- 1037885
- 3009077524
- 3019269298
- 2523676
- 9614683
- 3015612252
- 3011230048
- 8043903
- 3016851379
- 8020997
- 1220246
- 3015232217
- 3008403546
- 3002579136
- 3015910259
- 9710122
- 1054713
Source Documents#
Other 510(k) Records For Product Code IZI #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K261037 | 780 nm SPY Portable Handheld Imaging (SPY-PHI) System | Stryker Endoscopy | 2026-05-28 |
| K253181 | SURGIMAGE SIM 1000H Fluorescence Imaging Platform | Surgimage Corporation | 2026-05-13 |
| K243645 | IC-Flow™ Imaging System 2.0 | Diagnostic Green GmbH | 2025-09-22 |
| K243077 | Affirm 800 | Digital Surgery Systems, Inc. (D.B.A True Digital Surgery) | 2025-06-27 |
| K231986 | Modus IR | Synaptive Medical, Inc. | 2024-03-25 |
| K234090 | EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004) | Surgvision GmbH | 2024-03-20 |
| K231075 | Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option) | Carl Zeiss Meditec, Inc. | 2023-06-20 |
| K230727 | SPY Portable Handheld Imaging (SPY-PHI) System | Novadaq Technologies Ulc (A Part of Stryker) | 2023-06-05 |
| K222240 | EXPLORER AIR® II | Surgvision GmbH | 2023-02-28 |
| K214097 | Explorer Air II | Surgvision GmbH | 2022-02-25 |
| K202391 | DIR 800 | Aesculap, Inc. | 2021-01-21 |
| K192761 | Asimov-MKS Imaging System | Onlume, Inc. | 2020-01-17 |
| K190772 | SURGICAL MICROSCOPE SYSTEM ORBEYE with IR | Olympus Medical Systems Corp. | 2019-10-10 |
| K182907 | SPY Elite Intraoperative Perfusion Assessment System | Novadaq Technologies Ulc. (Now A Part of Stryker) | 2019-01-23 |
| K181537 | GLOW800 | Leica Microsystems (Schweiz) AG | 2018-09-07 |
Legacy Summary#
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FDA Review#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases