CIRCLE NEPHROSTOMY TUBE INTRODUCER— 510(k) K810533

Name: FDA 510(k) clearance K810533
Creator: U.S. Food and Drug Administration
Published: 1981-03-11

Substantially Equivalent

American V. Mueller

FDA 510(k) clearance K810533 for CIRCLE NEPHROSTOMY TUBE INTRODUCER, Substantially Equivalent on 1981-03-11. Applicant: American V. Mueller. Device class: 1.

Clearance details

Applicant: American V. Mueller
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1981-02-26
Decision date: 1981-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KOA

view all

K182664 — FiXcision2018-12-07
K950267 — URETHRAL SUTURE GUIDE1995-01-31
K932465 — LI VASECTOMY1994-03-02
K921546 — VASOVASOSTOMY SET1993-07-02
K931181 — VESITEC SUTURE PASSER1993-05-12

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.