HANCOCK * OBTURATORS— 510(k) K801885

Name: FDA 510(k) clearance K801885
Creator: U.S. Food and Drug Administration
Published: 1980-09-09

Substantially Equivalent

Hancock Laboratories, Inc.

FDA 510(k) clearance K801885 for HANCOCK * OBTURATORS, Substantially Equivalent on 1980-09-09. Applicant: Hancock Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Hancock Laboratories, Inc.
Product code: Code DTI
Device class: Class 1
Regulation: 21 CFR 870.3945
Advisory panel: Cardiovascular
Date received: 1980-08-07
Decision date: 1980-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K790534 — MERSILENE SUTURES1979-03-26
K780568 — DURAN FLEXIBLE RING1978-05-26

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