510(k) · Cleared

Cleared

Tech-Switch Electrosurgical Pencil, Single Use

K932345510(k) TraditionalCleared Apr 12, 1994333-day reviewClass II21 CFR 878.4400

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Conmedcorp · DWG Electrosurgical Device

Cleared on Apr 12, 1994 after a 333-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 1 later device descends from it.

Decided: Apr 12, 1994
Review: 333 days
Class: Class II
Product code: DWG
Recalls: None
Predicates: 0

1 later device descends from it, 1 citing it directly.

This deviceK932345 Tech-Switch Electrosurgical Pencil, Single UseConmedcorp · 1994
Descendant · cites it directly · 0 of its ownK042604 Vally Forge Scientific Malis Bipolar Disposable Finger Operated…Valley Forge Scientific Corp. · 2004

Most influential descendants

Showing 1 of 1 · See all

K042604Vally Forge Scientific Malis Bipolar Disposable Finger Operated Electrosurgical…Valley Forge Scientific Corp. · 2004 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K932345	Tech-Switch Electrosurgical Pencil, Single Use	Conmedcorp	1994	—
+1	K042604	Vally Forge Scientific Malis Bipolar Disposable Finger Operated…	Valley Forge Scientific Corp.	2004	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2004	1	0

FIG. 1 — Lineage of K932345, 1994–2004Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in DWG? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Candidate predicates for a device like this, rankedin the report
Recall history across each candidate’s familyin the report

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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K042604	Vally Forge Scientific Malis Bipolar Disposable Finger Operated Electrosurgical…	Valley Forge Scientific Corp.	2004	0

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

Of its descendants, K042604 (Valley Forge Scientific Corp., 2004) has gone furthest, with 0 descendants of its own.

How does its category compare?

All DWG devices

DWG Electrosurgical Device: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DWG

FDA has decided no DWG device since 2007.

Median 510(k) review, days · DWG

Too few DWG 510(k)s in any year since 2007 to give a median.

Recalls per year · DWG

No recall names DWG since 2007.

Adverse event reports per year · DWG

6in 2024

2007high 122 (2013) · low 0 (2007)2025

MAUDE reports naming product code DWG, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Median 510(k) review, days	MAUDE reports
2007	—	0
2008	—	0
2009	—	0
2010	—	5
2011	—	0
2012	—	13
2013	—	122
2014	—	84
2015	—	9
2016	—	0
2017	—	2
2018	—	1
2019	—	0
2020	—	0
2021	—	0
2022	—	0
2023	—	5
2024	—	6
2025	—	0
2026	—	—

https://510kreport.com/device/K932345 · printed Nov 4, 2026

Cite this page

510(k) Report. “K932345: Tech-Switch Electrosurgical Pencil, Single Use.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K932345

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Record history

FDA decision record loaded May 2, 2026
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026