ACCUTEX IM LATEX TEST— 510(k) K932551

Substantially Equivalent

J.S. Medical Assoc.

FDA 510(k) clearance K932551 for ACCUTEX IM LATEX TEST, Substantially Equivalent on 1993-08-09. Applicant: J.S. Medical Assoc.. Device class: 2.

Clearance details

Applicant: J.S. Medical Assoc.
Product code: Code KTN
Device class: Class 2
Regulation: 21 CFR 866.5640
Advisory panel: Immunology
Date received: 1993-05-26
Decision date: 1993-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Natick, MA, US

Download summary PDF View on FDA.gov ↗

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More clearances from J.S. Medical Assoc.

K932752 — VISI-SPOT1993-11-05
K932688 — EYE SPOT IM TEST1993-09-08
K932180 — EYE SPOT CRP TEST1993-08-23
K926112 — ACCUTEX BETA-HCG TEST1993-07-28
K924247 — ACCUTEX ASO LATEX TEST1992-12-07

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