Question 1

Who is the manufacturer of WEEVAC 6 INFANT EVACUATION STRETCHER?

Accepted Answer

W. Murphy Ent., Inc. filed the 510(k) submission for WEEVAC 6 INFANT EVACUATION STRETCHER (K902521).

Question 2

What is the FDA product code for WEEVAC 6 INFANT EVACUATION STRETCHER?

Accepted Answer

FPP. It is classified under 21 CFR 880.6900 as a Class 1 device in the General Hospital panel.

Question 3

When was WEEVAC 6 INFANT EVACUATION STRETCHER cleared by the FDA?

Accepted Answer

Jun 22, 1990 (decision: SESE).

Question 4

What is the regulatory pathway for WEEVAC 6 INFANT EVACUATION STRETCHER?

Accepted Answer

510(k) clearance (submission type: Traditional).

Question 5

Who can help prepare an FDA 510(k) submission like WEEVAC 6 INFANT EVACUATION STRETCHER?

Accepted Answer

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Record ID	K902521
Device Name	WEEVAC 6 INFANT EVACUATION STRETCHER
Applicant	W. Murphy Ent., Inc.
Product Code	FPP · General Hospital
Decision Date	Jun 22, 1990
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 880.6900
Device Class	Class 1

WEEVAC 6 INFANT EVACUATION STRETCHER

Device Facts

Regulatory Classification

Identification