510(k) K843732
- Device
- API UNISCEPT MIC
- Applicant
- ANALYTICAL PRODUCTS, INC.
- 510(k) number
- K843732
- Product code
- LTD
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-10-24
- Date received
- 1984-09-24
- Regulation
- 510(k) Premarket Notification
- Classification name
- Paraquat Assay
- 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
- Microbiology
- Device class
- 3
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- SUSAN D TIEDY
- Address
- 200 Express St. Plainview NY US 11803 11803
FDA Registration Numbers#
- 3031582440
Source Documents#
510(k) summary PDF not indicated by FDA
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