Cleared Traditional

K932036 - LACERATION TRAY

K932036 is an FDA 510(k) clearance for LACERATION TRAY, manufactured by Clinipad Corp.. The device is a Class 2 General Hospital device with product code FRG cleared through the Traditional 510(k) pathway after a 230-day FDA review.

K932036 · Clinipad Corp. · General Hospital
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Dec 1993
Decision
230d
Days
Class 2
Risk

K932036 is an FDA 510(k) clearance for the LACERATION TRAY. Classified as Wrap, Sterilization (product code FRG), Class II - Special Controls.

Submitted by Clinipad Corp. (Guilford, US). The FDA issued a Cleared decision on December 13, 1993 after a review of 230 days - an extended review cycle.

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. Standard predicate reliance. 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 Clinipad Corp. devices

FDA 510(k) Submission Details - K932036

510(k) Number K932036 FDA.gov
FDA Decision Cleared Substantially Equivalent - Special 510(k) (SESK)
Date Received April 27, 1993
Decision Date December 13, 1993
Days to Decision 230 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
101d slower than avg
Panel avg: 129d · This submission: 230d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FRG Device Classification - Class 2, Special Controls

Product Code FRG Wrap, Sterilization
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 - FRG Wrap, Sterilization

All 185
Devices cleared under the same product code (FRG) and FDA review panel - the closest regulatory comparables to K932036.
TRACHEOSTOMY CARE TRAY
K935685 · Cush Medical Products · Feb 1994
SKIN SCRUB TRAY
K935742 · Cush Medical Products · Feb 1994
CARAPACE DEBRIDEMENT KITS
K931669 · Carapace, Inc. · Feb 1994
CONVENIENCE CONTOUR KITS REDI NURSE SYSTEM
K933151 · Contour Fabricators of Florida, Inc. · Dec 1993
WRAPPEL T
K923408 · Standard Textile Co., Inc. · Apr 1993
CONVERTORS STERILIZATION WRAP
K921243 · Baxter Healthcare Corp · Oct 1992