GLOVES, FLOOR— 510(k) K780181

Substantially Equivalent

Tillotson Rubber Co., Inc.

FDA 510(k) clearance K780181 for GLOVES, FLOOR, Substantially Equivalent on 1978-02-21. Applicant: Tillotson Rubber Co., Inc.. Device class: 1.

Clearance details

Applicant: Tillotson Rubber Co., Inc.
Product code: Code FML
Device class: Class 1
Regulation: 21 CFR 880.6140
Advisory panel: General Hospital
Date received: 1978-02-03
Decision date: 1978-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FML

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More clearances from Tillotson Rubber Co., Inc.

K905765 — PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES)1991-02-25
K903756 — STERILE PATIENT EXAMINATION GLOVES1990-09-05
K903607 — POWDER FREE, NON-STERILE EXAMINATION GLOVES1990-08-17
K894828 — HPI ORTHO SURGEONS' GLOVE1990-05-07
K770704 — GLOVES, SURGEONS, LATEX1977-06-24

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