510(k) K902669
- Device
- BPA, BODY POSITION ALARM
- Applicant
- BAGRAD
- 510(k) number
- K902669
- Product code
- LZW
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1990-07-27
- Date received
- 1990-06-18
- Regulation
- 510(k) Premarket Notification
- Classification name
- Monitor, Spine Curvature
- Medical specialty
- 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
- Review panel
- Physical Medicine
- Device class
- U
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- SHAWN GALLAGHER
- Address
- 375 Glendening Rd. Orange Park FL US 32073 32073
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code LZW #
Legacy Summary#
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FDA Review#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases