DULTURE MEDIA, SELECTIVE & NON-DIFFER— 510(k) K820845

Name: FDA 510(k) clearance K820845
Creator: U.S. Food and Drug Administration
Published: 1982-04-16

Substantially Equivalent

Blue Ridge Media Co.

FDA 510(k) clearance K820845 for DULTURE MEDIA, SELECTIVE & NON-DIFFER, Substantially Equivalent on 1982-04-16. Applicant: Blue Ridge Media Co.. Device class: 1.

Clearance details

Applicant: Blue Ridge Media Co.
Product code: Code JSJ
Device class: Class 1
Regulation: 21 CFR 866.2360
Advisory panel: Microbiology
Date received: 1982-03-26
Decision date: 1982-04-16
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

More clearances from Blue Ridge Media Co.

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K820839 — CULTURE MEDIA, SINGLE BIOCHEM. TEST1982-04-16
K820840 — CULTURE MEDIA, GENERAL NUTRIENT BROTH1982-04-16
K820841 — CULTURE MEDIA, MULTIPLE BIOCHEMICAL1982-04-16
K820842 — CULTURE MEDIA, NON-SELECTIVE/DIFFER1982-04-16
K820843 — CULTURE MEDIA SELECTIVE BROTH1982-04-16

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.