Macon & Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Macon & Co., Inc. makes
Macon & Co., Inc. manufactures a fetal monitoring transducer strap, designed for continuous monitoring of fetal heart rate during pregnancy, and a surgical stitch cutter, used to safely and efficiently remove sutures post-operation.
The company’s products are regulated under the FDA’s 510(k) pathway, with devices classified as Class I and Class II. These products are listed in the FDA’s 510(k) clearance registry, and the manufacturer is based in the United States.
Catalogue
Fetal Monitoring Transducer Strap Ref K902802
Regimes: 510(k) Registry: 510(k)Surgical Stitch Cutter Ref K800103
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Macon & Co., Inc. have in the registry?
The registry currently lists 2 devices for Macon & Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Macon & Co., Inc.'s devices?
Among its 2 most recently registered devices, Macon & Co., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Macon & Co., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Macon & Co., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Macon & Co., Inc. in the registry?
The most recently registered devices listed for Macon & Co., Inc. include FETAL MONITORING TRANSDUCER STRAP and SURGICAL STITCH CUTTER.