OB/GYN DRAPE— 510(k) K920808

Substantially Equivalent

Preferred Medical Products

FDA 510(k) clearance K920808 for OB/GYN DRAPE, Substantially Equivalent on 1993-02-19. Applicant: Preferred Medical Products. Device class: 2.

Clearance details

Applicant: Preferred Medical Products
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1992-02-21
Decision date: 1993-02-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KKX

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K163556 — MediClear PreOp2017-09-14

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K904440 — LOCAL PLEXUS BLOCK ANESTHESIA CATHETER KITS1991-06-07
K885278 — EPIDURAL ANESTHESIA TRAY1989-03-16
K885277 — SPINAL ANESTHESIA TRAY1989-03-06

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