DRAPE STERICOVER— 510(k) K863512

Substantially Equivalent

Sterimed, Inc.

FDA 510(k) clearance K863512 for DRAPE STERICOVER, Substantially Equivalent on 1986-09-30. Applicant: Sterimed, Inc.. Device class: 2.

Clearance details

Applicant: Sterimed, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1986-09-09
Decision date: 1986-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Acworth, GA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KKX

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K163556 — MediClear PreOp2017-09-14

More clearances from Sterimed, Inc.

K900664 — DISPOSABLE COURNAND, SELDINGER & ONE-WALL NEEDLES1990-07-18
K853044 — STERICOVER1985-11-01

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