GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.— 510(k) K873257

Name: FDA 510(k) clearance K873257
Creator: U.S. Food and Drug Administration
Published: 1987-11-06

Substantially Equivalent

Central Media

FDA 510(k) clearance K873257 for GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA., Substantially Equivalent on 1987-11-06. Applicant: Central Media. Device class: 1.

Clearance details

Applicant: Central Media
Product code: Code JSG
Device class: Class 1
Regulation: 21 CFR 866.2300
Advisory panel: Microbiology
Date received: 1987-08-11
Decision date: 1987-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sacramento, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JSG

view all

K882495 — THIOGLYCOLLATE BROTH W/VITA. K & HEMIN - #T30071988-07-01
K881522 — DEXTROSE AGAR1988-04-18
K881523 — DEXTROSE TRYPTONE BROTH1988-04-18
K881525 — COOKED MEAT MEDIUM1988-04-18
K881528 — CASEIN PEPTONE, LOW VITAMIN1988-04-18

More clearances from Central Media

view all

K873258 — STREPTOCOCCAL SELECTIVE DIFFEREN. & ENRICHED MEDIA1987-11-06
K873259 — SPECIALTY MEDIA1987-11-06
K873260 — CORYNEBACTERIA ISOLATION MEDIA1987-11-06
K873267 — ECG BASED MEDIA1987-11-04
K873268 — MUELLER HINTON MEDIA1987-11-04

Adverse events under product code JSG

product code JSG

Malfunction: 817
Total: 817

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.