510(k) K955519

Device
ANALYTICAL REVIEW STATION
Applicant
CAMTRONICS, LTD.
510(k) number
K955519
Product code
IZI  
Decision
Substantially Equivalent (SESE)
Decision date
1996-05-09
Date received
1995-12-04
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
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
ROBERT KRIEDERMANN
Address
900 Walnut Ridge Dr. P.O. Box 950 Hartland WI US 53029 53029

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code IZI  

510(k)DeviceApplicantDecision date
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K243077Affirm 800Digital Surgery Systems, Inc. (D.B.A True Digital Surgery)2025-06-27
K231986Modus IRSynaptive Medical, Inc.2024-03-25
K234090EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)Surgvision GmbH2024-03-20
K231075Fluorescence Accessories (YELLOW 560 and INFRARED 800 with FLOW 800 Option)Carl Zeiss Meditec, Inc.2023-06-20
K230727SPY Portable Handheld Imaging (SPY-PHI) SystemNovadaq Technologies Ulc (A Part of Stryker)2023-06-05
K222240EXPLORER AIR® IISurgvision GmbH2023-02-28
K214097Explorer Air IISurgvision GmbH2022-02-25
K202391DIR 800Aesculap, Inc.2021-01-21
K192761Asimov-MKS Imaging SystemOnlume, Inc.2020-01-17
K190772SURGICAL MICROSCOPE SYSTEM ORBEYE with IROlympus Medical Systems Corp.2019-10-10
K182907SPY Elite Intraoperative Perfusion Assessment SystemNovadaq Technologies Ulc. (Now A Part of Stryker)2019-01-23
K181537GLOW800Leica Microsystems (Schweiz) AG2018-09-07
K180019CAAS WorkstationPie Medical Imaging BV2018-05-03

Legacy Summary

summary

FDA Review

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