510(k) K925588
- Device
- NORTEC STER SALINE-O.9% SODIUM CHLOR FOR DEV IRRI
- Applicant
- NORTH AMERICAN STERILIZATION & PACKAGING CO.
- 510(k) number
- K925588
- Product code
- LDQ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1993-12-03
- Date received
- 1992-11-05
- Regulation
- 510(k) Premarket Notification
- Classification name
- 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 Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products 510(k) Premarket Notification Var MP = { Version: '1.0.22', Domains: {'es':'esp.fda.gov'}, SrcLang: 'en', UrlLang: 'mp_js_current_la
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Clearance type
- Traditional
- Statement or summary
- Statement
- Third party reviewed
- No
Applicant Contact#
- Contact
- CHARLES E MEISCH
- Address
- 15 White Lake Rd. P.O. Box 923 Sparta NJ US 07871 07871
FDA Registration Numbers#
- 9611024
- 9616088
- 3008061617
- 3004111573
- 1061124
- 9610849
- 1423537
- 3004167615
- 1125615
Source Documents#
510(k) summary PDF not indicated by FDA
Legacy Summary#
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
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