ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE— 510(k) K874585

Name: FDA 510(k) clearance K874585
Creator: U.S. Food and Drug Administration
Published: 1987-12-02

Substantially Equivalent

Angiomed U.S., Inc.

FDA 510(k) clearance K874585 for ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE, Substantially Equivalent on 1987-12-02. Applicant: Angiomed U.S., Inc.. Device class: 1.

Clearance details

Applicant: Angiomed U.S., Inc.
Product code: Code DWO
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-11-09
Decision date: 1987-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

Download summary PDF View on FDA.gov ↗

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K913815 — AUTOMATED BIOPSY DEVICE, MODIFICATION1991-10-30
K890925 — MANAN BONE MARROW BIOPSY NEEDLE1989-04-11
K885145 — MEDSURG GREENE NEEDLE1989-03-14

More clearances from Angiomed U.S., Inc.

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K874771 — ANGIOMED INTRODUCING SETS1988-01-12
K864225 — ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT1987-01-30
K863386 — VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETS1986-10-24
K862805 — ANGIOMED VAC-U-CUT BIOPSY NEEDLE1986-09-29
K863446 — ANGIOMED HIGH PRESSURE CONNECTORS1986-09-23

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