Cleared Traditional

K893802 - PROVIEW SELF-SEALING STERILIZATION POUCH

K893802 is an FDA 510(k) clearance for PROVIEW SELF-SEALING STERILIZATION POUCH, manufactured by Cottrell, Ltd.. The device is a Class 2 General Hospital device with product code KCT cleared through the Traditional 510(k) pathway after a 317-day FDA review.

K893802 · Cottrell, Ltd. · General Hospital
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Optimized for regulatory review, auditing and printing
Apr 1990
Decision
317d
Days
Class 2
Risk

K893802 is an FDA 510(k) clearance for the PROVIEW SELF-SEALING STERILIZATION POUCH. Classified as Sterilization Wrap Containers, Trays, Cassettes & Other Accessories (product code KCT), Class II - Special Controls.

Submitted by Cottrell, Ltd. (Englewood, US). The FDA issued a Cleared decision on April 4, 1990 after a review of 317 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6850 - 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: Standard predicate-based submission. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Cottrell, Ltd. devices

FDA 510(k) Submission Details - K893802

510(k) Number K893802 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 22, 1989
Decision Date April 04, 1990
Days to Decision 317 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
188d slower than avg
Panel avg: 129d · This submission: 317d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KCT Device Classification - Class 2, Special Controls

Product Code KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6850
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 - KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

All 185
Devices cleared under the same product code (KCT) and FDA review panel - the closest regulatory comparables to K893802.
STERRAD STERILIZATION POUCH
K951295 · Advanced Sterilization Products · May 1995
BARRIER PLASTIC PACKAGING (MODIFICATION)
K933560 · Maxxim Medical · Apr 1994
SHAVE PREP TRAY
K935739 · Cush Medical Products · Feb 1994
CAM-WRAP(TM) NEW STERILIZATION PROCEDURE
K891983 · Medical Dynamics, Inc. · Apr 1989
THE KEYMED FIBERSCOPE STERILIZATION CASE
K860528 · Keymed, Inc. · Jul 1986
MICROVASIVE SILICONE SPRAY
K854063 · Microvasive · Oct 1985