FDA 510(k)

IDS SS-A/Ro; IDS SS-A/Ro 60 kDa; IDS SS-B/La

Numéro K : K253817 · 2026-08-21

DemandeurImmunodiagnostics Systems Limited

Date de décision2026-08-21

Code produitLLL

Comité consultatifIM

DécisionSubstantially Equivalent

Résumé du dispositif

IDS SS-A/Ro; IDS SS-A/Ro 60 kDa; IDS SS-B/La is the device name listed in this FDA 510(k) record. The listed applicant is Immunodiagnostics Systems Limited. It received FDA 510(k) clearance on 2026-08-21 under 510(k) number K253817. The device is classified under product code LLL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the IDS SS-A/Ro; IDS SS-A/Ro 60 kDa; IDS SS-B/La?

IDS SS-A/Ro; IDS SS-A/Ro 60 kDa; IDS SS-B/La is a medical device that received FDA 510(k) clearance on 2026-08-21. The listed applicant is Immunodiagnostics Systems Limited. The 510(k) number is K253817.

When did IDS SS-A/Ro; IDS SS-A/Ro 60 kDa; IDS SS-B/La receive FDA 510(k) clearance?

IDS SS-A/Ro; IDS SS-A/Ro 60 kDa; IDS SS-B/La received FDA 510(k) clearance on 2026-08-21, under 510(k) number K253817.

Who is the listed applicant for IDS SS-A/Ro; IDS SS-A/Ro 60 kDa; IDS SS-B/La?

The FDA 510(k) record lists Immunodiagnostics Systems Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IDS SS-A/Ro; IDS SS-A/Ro 60 kDa; IDS SS-B/La?

The FDA product code for IDS SS-A/Ro; IDS SS-A/Ro 60 kDa; IDS SS-B/La is LLL.

Dispositifs connexes (Code : LLL)

Les enregistrements connexes sont mis en correspondance automatiquement à l'aide des noms, codes produits ou autres métadonnées. Une mise en correspondance n'établit pas de relation clinique, scientifique, corporative ou réglementaire vérifiée ; veuillez consulter les sources officielles liées.

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Source officielle

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