Konigsberg Instruments, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Konigsberg Instruments, Inc. makes
Konigsberg Instruments, Inc. manufactures pressure transducers for angioplasty procedures, including the P51 model, and a range of esophageal motility probes (models P31–P38, P40–P43, and P50) designed for gastrointestinal function assessment.
These devices are classified under FDA’s Class I and Class II categories and are listed in the 510(k) registry. The company is based in the United States.
Catalogue
P51 Angioplasty Pressure Transducer Ref K813331
510(k) 510(k)- 510(k) 510(k)
Esophageal Motility Probe Ref K811083
510(k) 510(k)
Frequently asked questions
How many devices does Konigsberg Instruments, Inc. have in the registry?
The registry currently lists 3 devices for Konigsberg Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Konigsberg Instruments, Inc.'s devices?
Among its 3 most recently registered devices, Konigsberg Instruments, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Konigsberg Instruments, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Konigsberg Instruments, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Konigsberg Instruments, Inc. in the registry?
The most recently registered devices listed for Konigsberg Instruments, Inc. include P51 ANGIOPLASTY PRESSURE TRANSDUCER, MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50 and ESOPHAGEAL MOTILITY PROBE.