Cardinal Scale Mfg. Co.
Country not established FDA establishment FEI 1929045
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 1
Catalogue
Detecto Model 6700 Series Ref K924847
510(k) 510(k)
Company details
- FDA FEI number
- 1929045
- Address
- 102 EAST DAUGHERTY, Webb City, MO, 64870
FDA recalls
2015
- 23 Dec 2015 Z-2217-2017 Class II Terminated One complaint of a seat on a scale failing unexpectedly which can cause an injury.
Full distribution text
- 23 Dec 2015 Z-2217-2017 Class II Terminated One complaint of a seat on a scale failing unexpectedly which can cause an injury.
Frequently asked questions
How many devices does CARDINAL SCALE MFG. CO. have in the registry?
The registry currently lists 1 device for CARDINAL SCALE MFG. CO.. Devices recorded under merged duplicate company entries are counted once.
Which registries list CARDINAL SCALE MFG. CO.'s devices?
Among its 1 most recently registered device, CARDINAL SCALE MFG. CO. has devices listed in FDA 510(k) (1 device).
What risk classes do CARDINAL SCALE MFG. CO.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for CARDINAL SCALE MFG. CO.'s devices are Class I. Each device page shows its own class and authorisation.
Are there FDA recall records for CARDINAL SCALE MFG. CO.?
FDA recall records list 1 recall initiated by CARDINAL SCALE MFG. CO., the most recent initiated on 2015-12-23. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from CARDINAL SCALE MFG. CO. in the registry?
The most recently registered devices listed for CARDINAL SCALE MFG. CO. include DETECTO MODEL 6700 SERIES.