Cleared Traditional

K813024 - WA1000

K813024 is an FDA 510(k) clearance for WA1000, manufactured by Wallach Surgical Devices, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GEH cleared through the Traditional 510(k) pathway after a 36-day FDA review.

K813024 · Wallach Surgical Devices, Inc. · General & Plastic Surgery device
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Dec 1981
Decision
36d
Days
Class 2
Risk

K813024 is an FDA 510(k) clearance for the WA1000. Classified as Unit, Cryosurgical, Accessories (product code GEH), Class II - Special Controls.

Submitted by Wallach Surgical Devices, Inc. (Walker, US). The FDA issued a Cleared decision on December 3, 1981 after a review of 36 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4350 - the FDA general and plastic surgery 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 Wallach Surgical Devices, Inc. devices

FDA 510(k) Submission Details - K813024

510(k) Number K813024 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 28, 1981
Decision Date December 03, 1981
Days to Decision 36 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
79d faster than avg
Panel avg: 115d · This submission: 36d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GEH Device Classification - Class 2, Special Controls

Product Code GEH Unit, Cryosurgical, Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4350
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 & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GEH Unit, Cryosurgical, Accessories

All 115
Devices cleared under the same product code (GEH) and FDA review panel - the closest regulatory comparables to K813024.
HISTOFREEZER
K911420 · Solarcare Technologies Corp,Inc. · Jun 1991
WALLACH COLD SOAKER
K910491 · Wallach Surgical Devices, Inc. · May 1991
WCCS 800 WALLACH CARDIAC CRYOSURGICAL SYSTEM
K880416 · Wallach Surgical Devices, Inc. · Sep 1988
MODEL C2100-SERIES OPHTHALMIC CRYOPROBE
K810409 · Valleylab, Inc. · Mar 1981
LL100 CRYOSURGICAL SYSTEM
K803311 · Wallach Surgical Devices, Inc. · Feb 1981
CRYOSURGICAL DEVICE 2000
K781956 · Valleylab, Inc. · Jan 1979