SF BROTH— 510(k) K832615

Name: FDA 510(k) clearance K832615
Creator: U.S. Food and Drug Administration
Published: 1983-09-12

Substantially Equivalent

Carroll Biological Corp.

FDA 510(k) clearance K832615 for SF BROTH, Substantially Equivalent on 1983-09-12. Applicant: Carroll Biological Corp.. Device class: 1.

Clearance details

Applicant: Carroll Biological Corp.
Product code: Code JSJ
Device class: Class 1
Regulation: 21 CFR 866.2360
Advisory panel: Microbiology
Date received: 1983-07-08
Decision date: 1983-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JSJ

view all

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 Carroll Biological Corp.

view all

K832243 — CULTURE MEDIUM FOR ANTIMICROBIAL SUS1983-09-29
K832611 — TRYPTIC SOY AGAR1983-09-12
K832612 — CHOCOLATE AGAR & THAYER MARTIN AGAR1983-09-12
K832613 — MANNITOL SALT AGAR1983-09-12
K832614 — SELENITE BROTH1983-09-12

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.