Medline Admission Kits

FDA 510(k) K965107 · Medline Industries, Inc.

Substantially Equivalent

510(k) numberK965107

Submission

Device name
Medline Admission Kits
Applicant
Medline Industries, Inc.
Mundelein, IL, US
Received
December 20, 1996
Decision date
March 11, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FXX – Mask, Surgical
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4040
Specialty
General, Plastic Surgery

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Questions and answers

When was Medline Admission Kits cleared by the FDA?

Medline Admission Kits (K965107) received a 510(k) decision of Substantially Equivalent on March 11, 1997, 81 days after the submission was received.

What is the product code of K965107?

The FDA product code is FXX – Mask, Surgical, a Class II (moderate risk) device regulated under 21 CFR 878.4040.