Cleared Traditional

K810101 - WATER RESISTANT FOOTSWITCH W/CABLE

K810101 is an FDA 510(k) clearance for WATER RESISTANT FOOTSWITCH W/CABLE, manufactured by Aspen Laboratories, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GEI cleared through the Traditional 510(k) pathway after a 13-day FDA review.

K810101 · Aspen Laboratories, Inc. · General & Plastic Surgery device
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Jan 1981
Decision
13d
Days
Class 2
Risk

K810101 is an FDA 510(k) clearance for the WATER RESISTANT FOOTSWITCH W/CABLE. Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Aspen Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 29, 1981 after a review of 13 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4400 - 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 Aspen Laboratories, Inc. devices

FDA 510(k) Submission Details - K810101

510(k) Number K810101 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 16, 1981
Decision Date January 29, 1981
Days to Decision 13 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
102d faster than avg
Panel avg: 115d · This submission: 13d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GEI Device Classification - Class 2, Special Controls

Product Code GEI Electrosurgical, Cutting & Coagulation & Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4400
Definition Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
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 - GEI Electrosurgical, Cutting & Coagulation & Accessories

All 1260
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K810101.
PREGELLED DISPOS. ELECTROSURG. GROUND EL
K810277 · Conmedcorp · Mar 1981
DAVOL ELECTRO MEDICAL SYSTEMS
K810273 · C.R. Bard, Inc. · Mar 1981
ELECTROSURGICAL TIP CLEANER & HOLDER
K803055 · Devon Industries, Inc. · Feb 1981
BOUIE ELECTROSURGICAL TIP CLEANER
K802827 · Sybron Corp. · Dec 1980
ELECTRO SURGICAL TIP CLEANER
K802605 · Concept, Inc. · Nov 1980
VALLEYLAB RETURN ELECTRODE MONITOR
K801153 · Valleylab, Inc. · May 1980