Gespac, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Gespac, Inc. makes
Gespaç, Inc. manufactures automated sedimentation rate systems, including the SR30, SR50, and SR60 models, designed to measure erythrocyte sedimentation rate (ESR) in blood samples. These devices automate the traditional manual sedimentation test, providing quantitative results for clinical diagnostics.
The company’s automated sedimentation rate systems fall under Class I regulatory classification in the US. These devices are listed via 510(k) clearance with the FDA. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
SR30/SR50/SR60 Automated Sedimentation Rate Ref K890503
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gespac, Inc. have in the registry?
The registry currently lists 2 devices for Gespac, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gespac, Inc.'s devices?
Among its 2 most recently registered devices, Gespac, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Gespac, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gespac, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gespac, Inc. in the registry?
The most recently registered devices listed for Gespac, Inc. include SR30/SR50/SR60 AUTO SEDIMENT RATE SYSTEM, MODIFIED and SR30/SR50/SR60 AUTOMATED SEDIMENTATION RATE.