Fischer Industries, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Fischer Industries, Inc. makes
Fischer Industries, Inc. manufactures therapeutic ultrasound devices, including the Fischer/Krystal line, and processes X-ray film using automated systems like the Level 356 X-Ray Film Processor (Models MD & MD-D). These products are designed for medical imaging and therapeutic applications in clinical settings.
The company’s devices fall under FDA Class II regulation and are recorded in the 510(k) clearance registry. The portfolio is listed under U.S. FDA oversight, with no mention of international registries.
Catalogue
Fischer/Krystal Therapeutic Ultrasound Ref K861837
Regimes: 510(k) Registry: 510(k)X-Ray Film Processor Ref K940112
Regimes: 510(k) Registry: 510(k)Level 356 X-Ray Film Processor, Models Md & Md-D Ref K022154
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fischer Industries, Inc. have in the registry?
The registry currently lists 3 devices for Fischer Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fischer Industries, Inc.'s devices?
Among its 3 most recently registered devices, Fischer Industries, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Fischer Industries, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Fischer Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fischer Industries, Inc. in the registry?
The most recently registered devices listed for Fischer Industries, Inc. include FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND, X-RAY FILM PROCESSOR and LEVEL 356 X-RAY FILM PROCESSOR, MODELS MD & MD-D.