Cleared Traditional

K963494 - MORRISON MEDICAL DISPOSABLE RESTRAINT STRAP

K963494 is an FDA 510(k) clearance for MORRISON MEDICAL DISPOSABLE RESTRAINT STRAP, manufactured by Morrison Medical Products. The device is a Class 1 General Hospital device with product code FMQ cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K963494 · Morrison Medical Products · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1996
Decision
64d
Days
Class 1
Risk

K963494 is an FDA 510(k) clearance for the MORRISON MEDICAL DISPOSABLE RESTRAINT STRAP. Classified as Restraint, Protective (product code FMQ), Class I - General Controls.

Submitted by Morrison Medical Products (Libertyville, US). The FDA issued a Cleared decision on November 6, 1996 after a review of 64 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6760 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Morrison Medical Products devices

FDA 510(k) Submission Details - K963494

510(k) Number K963494 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 03, 1996
Decision Date November 06, 1996
Days to Decision 64 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
65d faster than avg
Panel avg: 129d · This submission: 64d
Pathway characteristics
Predicate-based equivalence.

FMQ Device Classification - Class 1, General Controls

Product Code FMQ Restraint, Protective
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6760
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - FMQ Restraint, Protective

All 121
Devices cleared under the same product code (FMQ) and FDA review panel - the closest regulatory comparables to K963494.
ANKLE RESTRAINT SYSTEM
K963416 · Morrison Medical Products · Nov 1996
POLYESTER PIL WRIST/ANKLE RESTRAINT/WRIST RESTRAINT UNIVERSAL/SOFT FLANNEL WRIST/ANKLE RESTRAINT/FOAM LIMB HOLDER
K963431 · Zimmer, Inc. · Nov 1996
ECONOMY SAFETY VEST RESTRAINT, SHOULDER TIE SAFETY VEST/SAFETY VEST RESTRAINT, HEAVY DUTY VEST RESTRAINT, MESH SAFETY VE
K963435 · Zimmer Patient Care Division · Nov 1996
HEELBO SECURITY BELT
K963060 · Heelbo, Inc. · Nov 1996
HEELBO PULLOVER PONCHO AND PULLOVER PONCHO WITH POCKET
K963099 · Heelbo, Inc. · Nov 1996
HEELBO PELVIC RESTRAINT
K963199 · Hollister, Inc. · Nov 1996