MICROPITETTE— 510(k) K792696

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K792696 for MICROPITETTE, Substantially Equivalent on 1980-02-01. Applicant: Meridian Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code JRC
Device class: Class 1
Regulation: 21 CFR 862.2050
Advisory panel: Clinical Chemistry
Date received: 1979-12-27
Decision date: 1980-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JRC

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K834100 — PRE-CALIBRATED PIPETTES1984-02-21
K822078 — DADE DISP. DISPENSING-SPREADING PIPETS1982-07-27
K770594 — LABORATORY EXPENDABLE PRODUCTS1977-07-06
K760621 — LANCER PLASTIC TRANSFER PIPETTE1976-10-05

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K984346 — PREMIER TYPE SPECIFIC HSV-2 IGG ELISA TEST1999-06-25
K983255 — MODIFICATION TO: PREMIER PLATINUM HPSA1998-12-17

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