TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHES— 510(k) K871483

Name: FDA 510(k) clearance K871483
Creator: U.S. Food and Drug Administration
Published: 1987-04-29

Substantially Equivalent

Isratech Marketing Corp.

FDA 510(k) clearance K871483 for TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHES, Substantially Equivalent on 1987-04-29. Applicant: Isratech Marketing Corp.. Device class: 1.

Clearance details

Applicant: Isratech Marketing Corp.
Product code: Code KIZ
Device class: Class 1
Regulation: 21 CFR 864.2240
Advisory panel: Hematology
Date received: 1987-04-15
Decision date: 1987-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KIZ

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K890542 — MULTIWELL CULTURE PLATE INSERTS1989-02-14
K873891 — TISSUE CULTURE DISHES1987-11-25
K854724 — CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE1985-12-13
K853634 — CORNING CELL WELLS-MULTIPLE WELL PLATES1985-09-16
K821687 — REMOVAWELL TISSUE CULTURE PLATE W/LID1982-06-24

More clearances from Isratech Marketing Corp.

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K896165 — STERILE HYPOALLERGENIC SURGEONS' GLOVES1989-11-22

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