Cleared Traditional

K802330 - HI-TEMP LOOPTIP SURGICAL CAUTERY

K802330 is the FDA 510(k) clearance for HI-TEMP LOOPTIP SURGICAL CAUTERY by Medical Products Development, Inc.. It is a Class 2 General & Plastic Surgery device (product code GEI) cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K802330 · Medical Products Development, Inc. · General & Plastic Surgery device
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Nov 1980
Decision
50d
Days
Class 2
Risk

K802330 is an FDA 510(k) clearance for the HI-TEMP LOOPTIP SURGICAL CAUTERY. Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Medical Products Development, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 12, 1980 after a review of 50 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 Medical Products Development, Inc. devices

Submission Details

510(k) Number K802330 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 23, 1980
Decision Date November 12, 1980
Days to Decision 50 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
65d faster than avg
Panel avg: 115d · This submission: 50d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 1179
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K802330.
ELECTROSURGICAL TIP CLEANER & HOLDER
K803055 · Devon Industries, Inc. · Feb 1981
WATER RESISTANT FOOTSWITCH W/CABLE
K810101 · Aspen Laboratories, Inc. · Jan 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
REUSABLE HAND-TROL
K800597 · Aspen Laboratories, Inc. · Apr 1980