MSI-DIFF PLUS— 510(k) K880270

Substantially Equivalent

Medical Specialties, Inc.

FDA 510(k) clearance K880270 for MSI-DIFF PLUS, Substantially Equivalent on 1988-03-01. Applicant: Medical Specialties, Inc.. Device class: 2.

Clearance details

Applicant: Medical Specialties, Inc.
Product code: Code JPK
Device class: Class 2
Regulation: 21 CFR 864.8625
Advisory panel: Hematology
Date received: 1988-01-21
Decision date: 1988-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South Plainfield, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JPK

K160586 — XN-L CHECK2016-12-22
K160588 — XN CHECK BF2016-12-22
K160590 — XN CHECK2016-12-22
K160606 — BC-5D Hematology Control2016-09-01
K141957 — XN CHECK BF2014-12-05

More clearances from Medical Specialties, Inc.

K946201 — STAND, INFUSION1995-04-18
K931947 — CHECKPOINT1993-06-18
K926095 — REFRACTROL-SP1993-01-26
K924926 — MSI-HCT1993-01-07
K896566 — MODIFIED FOX EXTRA GRAM NEGATIVE AND POSITIVE1990-02-09

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