Cleared Traditional

K914910 - DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SUR...

K914910 is the FDA 510(k) clearance for DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SUR... by Davol, Inc.. It is a Class 2 General & Plastic Surgery device (product code GEI) cleared through the Traditional 510(k) pathway after a 66-day FDA review.

K914910 · Davol, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1992
Decision
66d
Days
Class 2
Risk

K914910 is an FDA 510(k) clearance for the DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SURG REUSABLE). Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Davol, Inc. (Cranston, US). The FDA issued a Cleared decision on January 6, 1992 after a review of 66 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 Davol, Inc. devices

Submission Details

510(k) Number K914910 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 01, 1991
Decision Date January 06, 1992
Days to Decision 66 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
49d faster than avg
Panel avg: 115d · This submission: 66d
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 1118
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K914910.
MEDITRON AUTOMATIC ELECTRONIC INSUFF. MODEL AEI-15
K920071 · Medical Devices, Inc. · Jul 1992
MULTI USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT
K915204 · Conmedcorp · Jun 1992
GENESIS ELECTROSURGICAL UNIT
K920185 · Conmedcorp · Apr 1992
MODELS E2502B/E2525 REUSABLE HANDSWITCHING PENCILS
K914400 · Valleylab, Inc. · Oct 1991
LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE
K912637 · Dexide, Inc. · Oct 1991
IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003
K912229 · Dlp, Inc. · Sep 1991