LASER RBP LASER(RETINOL BINDING PROTEIN REAGENTS)— 510(k) K853261

Name: FDA 510(k) clearance K853261
Creator: U.S. Food and Drug Administration
Published: 1985-08-22

Substantially Equivalent

Behring Diagnostics, Inc.

FDA 510(k) clearance K853261 for LASER RBP LASER(RETINOL BINDING PROTEIN REAGENTS), Substantially Equivalent on 1985-08-22. Applicant: Behring Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Behring Diagnostics, Inc.
Product code: Code CZS
Device class: Class 1
Regulation: 21 CFR 866.5765
Advisory panel: Immunology
Date received: 1985-08-02
Decision date: 1985-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: La Jolla, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CZS

view all

K973189 — RETINOL BINDING PROTEIN RBP RID KIT1997-09-29
K955881 — RETINOL BINDING RID KIT1996-03-22

More clearances from Behring Diagnostics, Inc.

view all

K973832 — OPUS HLH CONTROLS1997-10-27
K972929 — N ANTISERUM TO HUMAN ALBUMIN1997-10-20
K972840 — N ANTISERUM TO HUMAN TRANSFERRIN1997-10-17
K973202 — MODIFICATION OF OPUS FERRITIN TEST SYSTEM1997-09-12
K972316 — OPUS D-DIMER1997-09-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.