SELECTIVE STREPTOCOCCUS AGAR— 510(k) K834005

Name: FDA 510(k) clearance K834005
Creator: U.S. Food and Drug Administration
Published: 1984-01-03

Substantially Equivalent

Micro Media Laboratories

FDA 510(k) clearance K834005 for SELECTIVE STREPTOCOCCUS AGAR, Substantially Equivalent on 1984-01-03. Applicant: Micro Media Laboratories. Device class: 1.

Clearance details

Applicant: Micro Media Laboratories
Product code: Code JSJ
Device class: Class 1
Regulation: 21 CFR 866.2360
Advisory panel: Microbiology
Date received: 1983-11-21
Decision date: 1984-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K882463 — POTATO DEXTROSE AGAR (PDA) - PRODUCT #P34211988-06-22
K881524 — DERMATOPHYTE TEST MEDIUM1988-04-18
K881526 — CHAPMAN STONE MEDIUM1988-04-18
K881530 — BRILLIANT GREEN AGAR W/SULFADIAZINE1988-04-18
K881544 — LITTMAN AGAR1988-04-18

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K853690 — COLUMBIZ BLOOD AGAR1985-09-17
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K851344 — OXIDATIVE FORMENTIVE MEDIUM1985-04-22
K851343 — BROM CRESOL PURPLE STARCH1985-04-19
K851345 — PURPLE BROTH1985-04-19

Adverse events under product code JSJ

product code JSJ

Malfunction: 520
Total: 520

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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