DUJOVNY MICROSURGICAL SCISSORS— 510(k) K810485

Name: FDA 510(k) clearance K810485
Creator: U.S. Food and Drug Administration
Published: 1981-02-27

Substantially Equivalent

American V. Mueller

FDA 510(k) clearance K810485 for DUJOVNY MICROSURGICAL SCISSORS, Substantially Equivalent on 1981-02-27. Applicant: American V. Mueller. Device class: 1.

Clearance details

Applicant: American V. Mueller
Product code: Code GZX
Device class: Class 1
Regulation: 21 CFR 882.4525
Advisory panel: Neurology
Date received: 1981-02-23
Decision date: 1981-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GZX

view all

K932169 — MICROSURGICAL INSTRUMENTS1993-07-20
K926048 — CLARUS ENDOSCOPIC BALL PROBE1993-04-07
K911932 — J105 JAMES SURGICAL SYSTEM I/A PACK1991-08-26
K890216 — MICROSURGICAL KERATOME1989-02-16
K873933 — RANGE OF NEUROSURGICAL INSTRUMENTS IN TITANIUM1987-12-17

More clearances from American V. Mueller

view all

K873771 — HEYER-SCHULTE(R) ONE PIECE SHUNT VENT. CATH. INTRO1987-12-18
K873332 — MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM1987-09-08
K871685 — HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS1987-06-12
K864676 — HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM1986-12-29
K862772 — V. MUELLER (R) GOOSENECK CIRCULAR STAPLER1986-08-18

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