Cleared Traditional

K772403 - CUT-DOWN BUILT-UP TOILET SEAT

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Feb 1978
Decision
56d
Days
-
Risk

K772403 is an FDA 510(k) clearance for the CUT-DOWN BUILT-UP TOILET SEAT.

Submitted by Fred Sammons, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 21, 1978 after a review of 56 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel. 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 Fred Sammons, Inc. devices

FDA 510(k) Submission Details - K772403

510(k) Number K772403 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 27, 1977
Decision Date February 21, 1978
Days to Decision 56 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
59d faster than avg
Panel avg: 115d · This submission: 56d
Pathway characteristics
Predicate-based equivalence.

LDQ Device Classification - Class ,

Product Code LDQ
Device Class -

Regulatory Peers - LDQ

All 23
Devices cleared under the same product code (LDQ) and FDA review panel - the closest regulatory comparables to K772403.
AMPCO SKIN SCRUB TRAYS, CAT.#SS612
K802044 · Associated Medical Products Co. · Sep 1980
TUBE HOLDER
K801421 · Devon Industries, Inc. · Jul 1980
CONPHAR SURGICAL RAZORR
K791798 · Conphar, Inc. · Feb 1980
ISOLATION KIT
K770381 · American Hospital Supply Corp. · Apr 1977
RAZOR, DISPOSABLE
K760328 · Devon Industries, Inc. · Aug 1976
RAZOR, SCHICK DISPOSABLE
K760342 · Parke-Davis Co. · Aug 1976