CEMENT DISPENSER CEMENT MIXER— 510(k) K790459

Name: FDA 510(k) clearance K790459
Creator: U.S. Food and Drug Administration
Published: 1979-03-28

Substantially Equivalent

Dow Corning Wright

FDA 510(k) clearance K790459 for CEMENT DISPENSER CEMENT MIXER, Substantially Equivalent on 1979-03-28. Applicant: Dow Corning Wright. Device class: 1.

Clearance details

Applicant: Dow Corning Wright
Product code: Code JSG
Device class: Class 1
Regulation: 21 CFR 866.2300
Advisory panel: Microbiology
Date received: 1979-03-05
Decision date: 1979-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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 Dow Corning Wright

view all

K932210 — ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT1994-09-07
K932911 — ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT1994-06-30
K934354 — LACEY ALL POLYETHYLENE TIBIAL COMPONENT1994-06-03
K932222 — SLT FEMORAL HEAD1994-05-27
K932858 — ORTHOLOC ADVANTIM TIBIAL BASE COMPONENT1994-02-16

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.