510(k) Report

510(k) · Cleared

Cleared

Dasky Disposable Sampling Tube (Model name: VSM02)

K211675510(k) TraditionalCleared Aug 8, 2022433-day reviewClass II21 CFR 866.2950

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

Ningbo Dasky Life Science Co., Ltd. · QBD Microbial Nucleic Acid Storage And Stabilization Device

Cleared on Aug 8, 2022 as substantially equivalent to K202641 (Zymo Research, 2020) after a 433-day review. Its family tree reaches back 2 generations to 2018.

Decided
Aug 8, 2022
Review
433 days
Class
Class II
Product code
QBD
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to DEN170029 (2018). No later device cites it as a predicate yet.

  1. Root · 2 generations backDEN170029 PrimeStore MTMLonghorn Vaccines and Diagnostics, LLC · 2018
  2. 1 generation backK202641 DNA/RNA Shield Collection TubeZymo Research · 2020
  3. This deviceK211675 Dasky Disposable Sampling Tube (Model name: VSM02)Ningbo Dasky Life Science Co., Ltd. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2DEN170029PrimeStore MTMLonghorn Vaccines and Diagnostics, LLC2018—
−1K202641DNA/RNA Shield Collection TubeZymo Research2020—
0 (this device)K211675Dasky Disposable Sampling Tube (Model name: VSM02)Ningbo Dasky Life Science Co., Ltd.2022—
FIG. 1 — Lineage of K211675, 2018–2022Source: 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 QBD? 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 QBD device

  1. #1 K202641 DNA/RNA Shield Collection Tubescore 18.5 · 1 generation · 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
*K202641DNA/RNA Shield Collection Tube
Summary page 4
…gulation Class: Class II Panel: Microbiology Product Code: QBD 3. Predicate Device 510(K) number: K202641 Device Name: DNA/RNA Shield Collection tube Manufacturer: Zymo Research Regulation Descr…
Zymo Research2020—

Also cleared against K202641: 5 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 4 years and passes through 3 companies; a new generation was cleared every 2.7 years on median.
  • None of the 2 ancestors has a recall.
  • 5 other devices also cite its predicate K202641.

How does its category compare?

All QBD devices

QBD Microbial Nucleic Acid Storage And Stabilization Device: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · QBD

1in 2025

2018: 12020: 22021: 12022: 22023: 52024: 52025: 1
2007high 5 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QBD

651in 2024

2023: 286 days median2024: 651 days median
2007high 651 (2024) · low 286 (2023)2026

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

Recalls per year · QBD

2in 2022

2022: 2, 2 Class I
2007high 2 (2022) · low 0 (2007)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · QBD

No MAUDE report names QBD since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20181—00
20190—00
20202—00
20211—00
20222—2 (2)0
2023528600
2024565100
20251—00
20260—0—

What is it indicated for?

The Dasky Disposable Sampling Tube (Model name: VSMO2) is intended for the stabilization, transportation and inactivation of infectious unprocessed nasopharyngeal specimen samples suspected of containing SARS-CoV-2. These devices can be used for collection transport and storage of specimens from the collection site to the laboratory. The specimens collected and stored in a Dasky Disposable Sampling Tube (Model name: VSMO2) are suitable for use with compatible laboratory based molecular diagnostic devices.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K211675: Dasky Disposable Sampling Tube (Model name: VSM02).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K211675

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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