Results for “N-ASSAY TIA MULTI V-NL”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED FDA 510(k) 5 FDA PMA GUDID

Country / market United States 5

Risk class Class I 1 Class IIa Class IIb Class III Class II (US) 4

More classes (11)

Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

Verified Validated only

Category (EMDN)

Browse by category

5 devices foundsorted by relevance

Clear all

Device · Manufacturer · Authorizations

N-Assay Tia Multi V-Nl

Crestat Diagnostics, Inc.,United States(FDA 510(k) applicant) Class II

Active 510(k) 510(k) II
4 variants
- N-Assay Tia Multi V-Nl K964298
- N-Assay Tia Multi V-Nl K964300
- N-Assay Tia Multi V-Nl K964301
N-Assay Tia Multi V-Nl

Crestat Diagnostics, Inc.,United States(FDA 510(k) applicant) Class I

Active 510(k) 510(k) I

Previous Next

Showing 1-5 of 5

deviCERTS Global Medical Device Regulatory Database

About [email protected]

Results for “N-ASSAY TIA MULTI V-NL”

Category (EMDN)

N-Assay Tia Multi V-Nl

N-Assay Tia Multi V-Nl