Ampcor, Inc.

United StatesFDA applicant, unverified

Devices: 15

Catalogue15

Newest first, rows 1-15 of 15

Search and filter all 15 devices

Infectious Mononucleosis Qik-Dot Im Dry Card Test Ref K922297

Active Regimes: 510(k) Registry: 510(k) Class:II
C Reactive Protein Liquid Ref K892146

Active Regimes: 510(k) Registry: 510(k) Class:II
Rpr Test For Syphilis In Serum Or Plasma Ref K880477

Active Regimes: 510(k) Registry: 510(k) Class:II
Dipstick Salmonella Ref K910438

Active Regimes: 510(k) Registry: 510(k) Class:II
Single And Dual Band Dipstick Hcg Test Ref K893873

Active Regimes: 510(k) Registry: 510(k) Class:II
Infectious Mononucleosis (Im) Card & Liquid Test Ref K880148

Active Regimes: 510(k) Registry: 510(k) Class:II
Quik-Dot Toxoplasmosis Ref K890048

Active Regimes: 510(k) Registry: 510(k) Class:II
Quik-Dot C Reactive Protein Ref K892119

Active Regimes: 510(k) Registry: 510(k) Class:II
Rf Card Test & Rf Liquid Test Ref K880164

Active Regimes: 510(k) Registry: 510(k) Class:II
Group A Strep, Beta-Strep Ref K884750

Active Regimes: 510(k) Registry: 510(k) Class:I
Pregnancy (Hcg) Card & Liquid Test Ref K880163

Active Regimes: 510(k) Registry: 510(k) Class:II
Imfectious Mononucleosis Im Liquid Card Test Ref K922296

Active Regimes: 510(k) Registry: 510(k) Class:II
Pregnancy Beta-Hcg Card & Liquid Test Ref K880478

Active Regimes: 510(k) Registry: 510(k) Class:II
Trust Rpr Test For Syphilis In Serum Or Plasma Ref K880165

Active Regimes: 510(k) Registry: 510(k) Class:II
Quik-Dot Antistreptolysin-O Ref K890025

Active Regimes: 510(k) Registry: 510(k) Class:I

Rows 1-15 of 15

Frequently asked questions

How many devices does Ampcor, Inc. have in the registry?

The registry currently lists 15 devices for Ampcor, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ampcor, Inc.'s devices?

Among its 15 most recently registered devices, Ampcor, Inc. has devices listed in FDA 510(k) (15 devices).

What risk classes do Ampcor, Inc.'s devices fall under?

Among its 15 most recently registered devices, the classes recorded for Ampcor, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Ampcor, Inc. in the registry?

The most recently registered devices listed for Ampcor, Inc. include INFECTIOUS MONONUCLEOSIS QIK-DOT IM DRY CARD TEST, C REACTIVE PROTEIN LIQUID, RPR TEST FOR SYPHILIS IN SERUM OR PLASMA and DIPSTICK SALMONELLA.

Generated automatically from registry data and not verified by a human reviewer.

Catalogue15

Infectious Mononucleosis Qik-Dot Im Dry Card Test Ref K922297

C Reactive Protein Liquid Ref K892146

Rpr Test For Syphilis In Serum Or Plasma Ref K880477

Dipstick Salmonella Ref K910438

Single And Dual Band Dipstick Hcg Test Ref K893873

Infectious Mononucleosis (Im) Card & Liquid Test Ref K880148

Quik-Dot Toxoplasmosis Ref K890048

Quik-Dot C Reactive Protein Ref K892119

Rf Card Test & Rf Liquid Test Ref K880164

Group A Strep, Beta-Strep Ref K884750

Pregnancy (Hcg) Card & Liquid Test Ref K880163

Imfectious Mononucleosis Im Liquid Card Test Ref K922296

Pregnancy Beta-Hcg Card & Liquid Test Ref K880478

Trust Rpr Test For Syphilis In Serum Or Plasma Ref K880165

Quik-Dot Antistreptolysin-O Ref K890025

Frequently asked questions