Sparco, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Sparco, Inc. makes
Sparco, Inc. manufactures medical devices including LIMB-GUARD, FLASH GUARD PLASTIC VERSION, SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLE, SPARCO SCOPE GUARD, FLASH GUARD, and MASTER-GUARD, which are protective covers and poles used in medical settings.
The company's products are classified as Class I and Class II devices and are listed in the FDA 510(k) registry. Sparco, Inc. is based in the US.
Catalogue
Limb-Guard Ref K863964
Regimes: 510(k) Registry: 510(k)Flash Guard Plastic Version Ref K844286
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Sparco Scope Guard Ref K850268
Regimes: 510(k) Registry: 510(k)Flash Guard Ref K841669
Regimes: 510(k) Registry: 510(k)Master-Guard Ref K884041
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sparco, Inc. have in the registry?
The registry currently lists 6 devices for Sparco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sparco, Inc.'s devices?
Among its 6 most recently registered devices, Sparco, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Sparco, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Sparco, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sparco, Inc. in the registry?
The most recently registered devices listed for Sparco, Inc. include LIMB-GUARD, FLASH GUARD PLASTIC VERSION, SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLE and SPARCO SCOPE GUARD.