MEDSURG GREENE NEEDLE— 510(k) K885145

Substantially Equivalent

Medsurg Industries, Inc.

FDA 510(k) clearance K885145 for MEDSURG GREENE NEEDLE, Substantially Equivalent on 1989-03-14. Applicant: Medsurg Industries, Inc.. Device class: 1.

Clearance details

Applicant: Medsurg Industries, Inc.
Product code: Code DWO
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1988-12-15
Decision date: 1989-03-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Herndon, VA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DWO

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K921418 — ULTRA-CORE BIOPSY NEEDLES1992-06-19
K913815 — AUTOMATED BIOPSY DEVICE, MODIFICATION1991-10-30
K890925 — MANAN BONE MARROW BIOPSY NEEDLE1989-04-11
K885149 — NEEDLE INSERT FOR SOFT TISSUE BIOPSY DEVICE1989-01-26

More clearances from Medsurg Industries, Inc.

K920780 — MEDSURG INSERTION TRAY1994-08-19
K940175 — MEDSURG STERILE O.R. TOWELS1994-05-26
K934731 — MEDSURG STERILE IMAGING PRODUCTS1994-03-28
K925558 — INFILTUBE1994-03-04
K934971 — STERILE LAPAROTOMY SPONGES1994-02-07

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