PRESSURIZER, EXETER CEMENT— 510(k) K781792

Substantially Equivalent

Howmedica Corp.

FDA 510(k) clearance K781792 for PRESSURIZER, EXETER CEMENT, Substantially Equivalent on 1979-02-08. Applicant: Howmedica Corp.. Device class: 1.

Clearance details

Applicant: Howmedica Corp.
Product code: Code KIZ
Device class: Class 1
Regulation: 21 CFR 864.2240
Advisory panel: Hematology
Date received: 1978-10-25
Decision date: 1979-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KIZ

K890542 — MULTIWELL CULTURE PLATE INSERTS1989-02-14
K873891 — TISSUE CULTURE DISHES1987-11-25
K871483 — TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHES1987-04-29
K854724 — CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATE1985-12-13
K853634 — CORNING CELL WELLS-MULTIPLE WELL PLATES1985-09-16

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K980926 — DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATION1998-12-16
K980626 — DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATION1998-12-11

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