COUGH PILLOW— 510(k) K893809

Substantially Equivalent

Custom Hospitals Products

FDA 510(k) clearance K893809 for COUGH PILLOW, Substantially Equivalent on 1989-08-28. Applicant: Custom Hospitals Products. Device class: 1.

Clearance details

Applicant: Custom Hospitals Products
Product code: Code KMO
Device class: Class 1
Regulation: 21 CFR 880.5160
Advisory panel: General Hospital
Date received: 1989-05-22
Decision date: 1989-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KMO

K921852 — 4 SURE TM RECTAL TUBE1993-10-08
K883214 — THORACIC SUPPORT SYSTEM1989-01-17
K882592 — HEART HUGGER STERNUM SUPPORT HARNESS1988-09-20
K792629 — STERILIZATION PROCESS/T-BINDER1980-01-11

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