LASER STANDARD SERUM— 510(k) K761235

Substantially Equivalent

Behring Diagnostics, Inc.

FDA 510(k) clearance K761235 for LASER STANDARD SERUM, Substantially Equivalent on 1976-12-30. Applicant: Behring Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Behring Diagnostics, Inc.
Product code: Code JZW
Device class: Class 1
Regulation: 21 CFR 866.4540
Advisory panel: Immunology
Date received: 1976-12-10
Decision date: 1976-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JZW

K001647 — BN PROSPEC SYSTEM2000-09-26
K761234 — BEHRING LASER NEPHELOMETER1990-06-07
K892223 — BEHRING NEPHELOMETER 1001989-05-04
K873401 — TURBOX1987-09-23
K873407 — RRT SYSTEM LASER REFLECTOMETER ANALYZER1987-09-23

More clearances from Behring Diagnostics, Inc.

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.