CYTOMEGILISH TEST KIT— 510(k) K781392

Substantially Equivalent

Microbiological Assoc.

FDA 510(k) clearance K781392 for CYTOMEGILISH TEST KIT, Substantially Equivalent on 1978-10-24. Applicant: Microbiological Assoc.. Device class: 2.

Clearance details

Applicant: Microbiological Assoc.
Product code: Code GOK
Device class: Class 2
Regulation: 21 CFR 866.3510
Advisory panel: Microbiology
Date received: 1978-08-10
Decision date: 1978-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GOK

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K810835 — RUBAZYME - M1981-05-05
K792635 — ANTIBODY TO RUBELLA VIRUS1980-03-19
K792133 — RUBELISA TEST KIT1980-01-11
K790122 — RUBANON1979-02-15

More clearances from Microbiological Assoc.

K791397 — HERPES EIA TEST KIT1979-09-24
K781549 — TOXELISA TEST KIT1978-12-07
K780996 — RUBELISA TEST KIT1978-11-22
K781143 — IMMUNOFLUORESCENCE TEST KIT1978-08-14
K770764 — TISSUE CULTURE MEDIA W/HEPES BUFFER1977-07-21

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