510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K061721Substantially Equivalent

Pedi-Spider Strap

Emergency Products & Research, Inc., Kent OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K061721 is the FDA 510(k) clearance record for PEDI-SPIDER STRAP, a class I device, cleared for Emergency Products and Research on under FDA product code NZD (Stretcher, Patient Restraint). FDA's definition for product code NZD reads: "Soft restraints to be attached to a backboard or stretcher in order to immobilize the patient in emgency situations". FDA records list one 510(k) clearance for Emergency Products and Research. As of , FDA records show no recalls naming K061721.

Clearance record

Decision date
Received
(59 days to decision)
Product code
NZD Stretcher, Patient Restraint
Regulation
21 CFR 880.6900
Device class
Class I
Review panel
General Hospital
Applicant
Emergency Products and Research 890 W. Main St., Kent OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NZD

Trailing 12 months

FDA records hold no clearances under product code NZD in the trailing twelve months.

FDA records show no clearances under product code NZD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NZD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260