DRIPRIDE DISPOSABLE UNDERPAD— 510(k) K881859

Substantially Equivalent

Weyerhaeuser Co.

FDA 510(k) clearance K881859 for DRIPRIDE DISPOSABLE UNDERPAD, Substantially Equivalent on 1988-06-03. Applicant: Weyerhaeuser Co.. Device class: 1.

Clearance details

Applicant: Weyerhaeuser Co.
Product code: Code KME
Device class: Class 1
Regulation: 21 CFR 880.6060
Advisory panel: General Hospital
Date received: 1988-05-03
Decision date: 1988-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KME

K042145 — READY-HEAT BLANKET2004-09-17
K944953 — OREX MEDICAL BEDDING1994-12-02
K933636 — DISPOSE-A-SHEET1994-01-26
K932539 — DOCTOR DOWN --RESCUE WRAP1993-11-02
K922143 — AMERICAN BURN SHEET1992-08-10

More clearances from Weyerhaeuser Co.

K883894 — DRIPRIDE PROVIDE SLIM1989-01-30
K883895 — DRIPRIDE ULTRA INCONTINENT PAD1989-01-30
K872059 — DRIPRIDE PROVIDE ULTRA1988-03-16
K871725 — DRIPRIDE DISPOSABLE UNDERPADS1987-05-15
K854408 — ADULT ABSORBENT INCONTINENT BRIEF1985-11-19

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