Cleared Traditional

K821356 - DESERET CAPACITY PLUS ELECTROSURG. PAD

K821356 is the FDA 510(k) clearance for DESERET CAPACITY PLUS ELECTROSURG. PAD by Warner-Lambert Co.. It is a Class 2 General & Plastic Surgery device (product code GEI) cleared through the Traditional 510(k) pathway after a 69-day FDA review.

K821356 · Warner-Lambert Co. · General & Plastic Surgery device
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Jul 1982
Decision
69d
Days
Class 2
Risk

K821356 is an FDA 510(k) clearance for the DESERET CAPACITY PLUS ELECTROSURG. PAD. Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Warner-Lambert Co. (Mchenry, US). The FDA issued a Cleared decision on July 14, 1982 after a review of 69 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 Warner-Lambert Co. devices

Submission Details

510(k) Number K821356 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 1982
Decision Date July 14, 1982
Days to Decision 69 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
46d faster than avg
Panel avg: 115d · This submission: 69d
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 1130
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K821356.
DISP. METAL & PLASTIC ELECTROSURG. DEV
K822355 · Valleylab, Inc. · Sep 1982
CONDUCTIVE ADHESIVE DISPERSIVE ELECTRO
K822405 · Edward Weck, Inc. · Sep 1982
POLYHESIVE PATIENT RETURN ELECTRODE
K822572 · Valleylab, Inc. · Sep 1982
DIATHERMIC HANDLE FOR BIOPSY FORCEPS
K820971 · Mill-Rose Laboratory · Apr 1982
HOT BIOPSY FORCEPS W/ROUND CUPS
K820983 · Mill-Rose Laboratory · Apr 1982
SYBRON BOVIE CSV HAND CONTR. ELECTROSURG
K820494 · Sybron Corp. · Apr 1982