RETRACTING PROBES— 510(k) K811759

Name: FDA 510(k) clearance K811759
Creator: U.S. Food and Drug Administration
Published: 1981-07-20

Substantially Equivalent

American V. Mueller

FDA 510(k) clearance K811759 for RETRACTING PROBES, Substantially Equivalent on 1981-07-20. Applicant: American V. Mueller. Device class: 1.

Clearance details

Applicant: American V. Mueller
Product code: Code GAD
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1981-06-22
Decision date: 1981-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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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

Adverse events under product code GAD

product code GAD

Malfunction: 504
Total: 504

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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