510(k) Report

510(k) · Cleared

Cleared

P&P Safety Syringe

K043419510(k) TraditionalCleared Apr 15, 2005123-day reviewClass II21 CFR 880.5860

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

Medexel Medical Mfg. Co., Ltd. · MEG Syringe, Antistick

Cleared on Apr 15, 2005 as substantially equivalent to K031163 (Sez Corporation, 2003) after a 123-day review. Its family tree reaches back 2 generations to 2003.

Decided
Apr 15, 2005
Review
123 days
Class
Class II
Product code
MEG
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K011754 (2003). No later device cites it as a predicate yet.

  1. Root · 2 generations backK011754 Exel Securetouch PTP SyringeExelint Intl. Co. · 2003
  2. 1 generation backK031163 Sez Safety SyringeSez Corporation · 2003
  3. This deviceK043419 P&P Safety SyringeMedexel Medical Mfg. Co., Ltd. · 2005
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K011754Exel Securetouch PTP SyringeExelint Intl. Co.2003—
−1K031163Sez Safety SyringeSez Corporation2003—
0 (this device)K043419P&P Safety SyringeMedexel Medical Mfg. Co., Ltd.2005—
FIG. 1 — Lineage of K043419, 2003–2005Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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

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

Top candidate predicates for a new MEG device

  1. #1 K192551 1ml Luer Slip or Luer Lock Syringe, Syringe…score 19.6 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K031163Sez Safety Syringe
Summary page 1
…ry-Trade Name: p&p Safety Syringe Classification Name: Piston Syringe Common/Usual Name: Safety Syringe 2) Equivalent legally marketed device: SEZ safety syringe [K031163] 3) Indications for Use (intended use) . This device is a safety hypodermic syringe for intramuscular and subcutaneous inject…
Sez Corporation2003—

Also cleared against K031163: 3 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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?

  • The line of descent spans 2 years and passes through 3 companies; a new generation was cleared every 1.8 years on median.
  • None of the 2 ancestors has a recall.
  • 3 other devices also cite its predicate K031163.

How does its category compare?

All MEG devices

MEG Syringe, Antistick: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MEG

1in 2025

2007: 82008: 42009: 22010: 22011: 52012: 52013: 12014: 52015: 72016: 32017: 32018: 12019: 42020: 42021: 52022: 132023: 52025: 12026 (partial year): 1
2007high 13 (2022) · low 0 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MEG

229in 2023

2007: 100 days median2008: 145 days median2011: 113 days median2012: 109 days median2014: 153 days median2015: 253 days median2016: 179 days median2017: 130 days median2019: 249 days median2020: 296 days median2021: 152 days median2022: 216 days median2023: 229 days median
2007high 296 (2020) · low 100 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · MEG

1in 2024

2008: 12010: 12013: 52015: 12024: 1, 1 Class I
2007high 5 (2013) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · MEG

148in 2025

2007: 212008: 202009: 262010: 342011: 342012: 222013: 272014: 362015: 512016: 942017: 1812018: 2692019: 4972020: 3532021: 5412022: 1702023: 1202024: 1122025: 148
2007high 541 (2021) · low 20 (2008)2025

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

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20078100021
20084145120
20092—026
20102—134
20115113034
20125109022
20131—527
20145153036
20157253151
20163179094
201731300181
20181—0269
201942490497
202042960353
202151520541
2022132160170
202352290120
20240—1 (1)112
20251—0148
20261—0—

What is it indicated for?

This device is a safety hypodermic syringe for intramuscular and subcutaneous injection of

medication to patients. This device aids in prevention of needlestick injuries.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K043419: P&P Safety Syringe.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K043419

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026