Cleared Traditional

K800022 - MODEL 807 SUCTION CAUTERY FINGER TIP

K800022 is an FDA 510(k) clearance for MODEL 807 SUCTION CAUTERY FINGER TIP, manufactured by Malibu Laboratories. The device is a Class 2 General & Plastic Surgery device with product code GEI cleared through the Traditional 510(k) pathway after a 35-day FDA review.

K800022 · Malibu Laboratories · General & Plastic Surgery device
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Feb 1980
Decision
35d
Days
Class 2
Risk

K800022 is an FDA 510(k) clearance for the MODEL 807 SUCTION CAUTERY FINGER TIP. Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Malibu Laboratories (Mchenry, US). The FDA issued a Cleared decision on February 11, 1980 after a review of 35 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 Malibu Laboratories devices

FDA 510(k) Submission Details - K800022

510(k) Number K800022 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 07, 1980
Decision Date February 11, 1980
Days to Decision 35 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
80d faster than avg
Panel avg: 115d · This submission: 35d
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 2023
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K800022.
VALLEYLAB RETURN ELECTRODE MONITOR
K801153 · Valleylab, Inc. · May 1980
HYFRECATOR, #733
K800617 · Birtcher Corp. · May 1980
REUSABLE HAND-TROL
K800597 · Aspen Laboratories, Inc. · Apr 1980
DIATHERMIC SNARE (CRESENT TYPE)
K792343 · Mill-Rose Laboratory · Dec 1979
A.D.E. ASPEN DISPERSIVE ELECTRODE
K792315 · Zimmer, Inc. · Nov 1979
SAFE RETURN COT. #9675 & CONNECTOR ADAPT
K792044 · Concept, Inc. · Nov 1979