Cleared Traditional

K874296 - INFECTION CONTROL GOGGLE (TSE FONG)/STER/NON-STER

K874296 is an FDA 510(k) clearance for INFECTION CONTROL GOGGLE (TSE FONG)/STE..., manufactured by Ulti-Med Intl., Inc.. The device is a Class 2 General Hospital device with product code FXX cleared through the Traditional 510(k) pathway after a 79-day FDA review.

K874296 · Ulti-Med Intl., Inc. · General Hospital
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Jan 1988
Decision
79d
Days
Class 2
Risk

K874296 is an FDA 510(k) clearance for the INFECTION CONTROL GOGGLE (TSE FONG)/STER/NON-STER. Classified as Mask, Surgical (product code FXX), Class II - Special Controls.

Submitted by Ulti-Med Intl., Inc. (Schaumburg, US). The FDA issued a Cleared decision on January 7, 1988 after a review of 79 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 878.4040 - 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 Ulti-Med Intl., Inc. devices

FDA 510(k) Submission Details - K874296

510(k) Number K874296 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 20, 1987
Decision Date January 07, 1988
Days to Decision 79 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
50d faster than avg
Panel avg: 129d · This submission: 79d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FXX Device Classification - Class 2, Special Controls

Product Code FXX Mask, Surgical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4040
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - FXX Mask, Surgical

All 489
Devices cleared under the same product code (FXX) and FDA review panel - the closest regulatory comparables to K874296.
TECNOL FLUID SHIELD SURGICAL MASK W/EYEGUARD
K880757 · Tecnol New Jersey Wound Care, Inc. · Mar 1988
KLEENSPEC DISPOSABLE FACE SHIELD, MODEL 57001
K875194 · Welch Allyn, Inc. · Jan 1988
SAFETY SHIELD KIT
K873731 · Ballard Medical Products · Jan 1988
TECNOL FLUID SHIELD SURGICAL MASK
K874608 · Tecnol New Jersey Wound Care, Inc. · Dec 1987
TECNOL FOG-FREE SURGICAL MASK W/DERMA-TOUCH TAPE
K873785 · Tecnol New Jersey Wound Care, Inc. · Nov 1987
TECNOL CLASSIC CONE MASK
K870056 · Tecnol New Jersey Wound Care, Inc. · Feb 1987