510(k) Report

510(k) · Cleared

Cleared

Bloodstop and Bloodstop IX Hemostatic Gauze, Models BS-10,BS-11,BS-12,B-13, BS-IX27, BS-IX-14, Bsix-15, Bsix-17

K071578510(k) TraditionalCleared Sep 27, 2007111-day reviewClass U

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

Lifescience Plus, Inc. · QSY Hemostatic Wound Dressing Without Thrombin Or Other Biologics

Cleared on Sep 27, 2007 as substantially equivalent to K010933 (Alltracel Pharma, Ltd., 2002) after a 111-day review. Its family tree reaches back 3 generations to 1995. 3 later devices descend from it.

Decided
Sep 27, 2007
Review
111 days
Class
Class U
Product code
QSY
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K953781 (1995). 5 ancestors in all. 3 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2000: 1 other ancestor1999: 1 other ancestor2008: 1 descendant cleared2012: 1 descendant cleared2016: 1 descendant clearedK953781 · Innovative Technologies Calcium Alginate Wound Dressings · Innovative Technologies, Ltd. · 1995K980989 · 3M Tegagen HI Alginate Dressing & 3M Tegagen HG Alginate Dressing · Innovative Technologies, Ltd. · 1998K010933 · Seal-on Topical Hempstatic Powder Spray · Alltracel Pharma, Ltd. · 20021995200020052010201520202025
  1. Root · 3 generations backK953781 Innovative Technologies Calcium Alginate Wound DressingsInnovative Technologies, Ltd. · 1995
  2. 2 generations backK980989 3M Tegagen HI Alginate Dressing & 3M Tegagen HG Alginate DressingInnovative Technologies, Ltd. · 1998
  3. 1 generation backK010933 Seal-on Topical Hempstatic Powder SprayAlltracel Pharma, Ltd. · 2002
  4. This deviceK071578 Bloodstop and Bloodstop IX Hemostatic Gauze, Models…Lifescience Plus, Inc. · 2007
  5. Descendant · cites it directly · 0 of its ownK160679 WoundClot9Core Scientific Creation, Ltd. · 2016
  6. Descendant · cites it directly · 0 of its ownK112800 Suntouch Topical Hemostatic DressingHuizhou Foryou Medical Devices Co., Ltd. · 2012 · Recalled
  7. Descendant · cites it directly · 0 of its ownK082601 UltraClot, UltraClot OTCEmergency Medical Devices, LLC · 2008

Most influential descendants

Showing 3 of 3 · See all
  • K160679WoundClot9Core Scientific Creation, Ltd. · 2016 · cites it directly0descendants
  • K112800Suntouch Topical Hemostatic DressingHuizhou Foryou Medical Devices Co., Ltd. · 2012 · cites it directly0descendants
  • K082601UltraClot, UltraClot OTCEmergency Medical Devices, LLC · 2008 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K953781Innovative Technologies Calcium Alginate Wound DressingsInnovative Technologies, Ltd.1995—
−2K9809893M Tegagen HI Alginate Dressing & 3M Tegagen HG Alginate DressingInnovative Technologies, Ltd.1998—
−1K010933Seal-on Topical Hempstatic Powder SprayAlltracel Pharma, Ltd.2002—
0 (this device)K071578Bloodstop and Bloodstop IX Hemostatic Gauze, Models BS-10,BS-11,BS-12,B-13…Lifescience Plus, Inc.2007—
+1K160679WoundClot9Core Scientific Creation, Ltd.2016—
+1K112800Suntouch Topical Hemostatic DressingHuizhou Foryou Medical Devices Co., Ltd.20121
+1K082601UltraClot, UltraClot OTCEmergency Medical Devices, LLC2008—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199910
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200810
201210
201610
FIG. 1 — Lineage of K071578, 1995–2016Source: 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 QSY? 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 QSY device

  1. #1 K240713 Traumagel®score 15.0 · 5 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
*K010933Seal-on Topical Hempstatic Powder Spray
Summary page 5
…Common Name: Hemostatic wound dressing Product Code: FRO, unclassified 5. Predicate Device: Seal-On Hemostatic Powder Spray, K010933 6. Device Description and Intended Use: BloodSTOP and BloodSTOP iX Hemostatic Gauze are made from regenerat…
Alltracel Pharma, Ltd.2002—

Also cleared against K010933: 5 other devices →

What descends from it? (3)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K160679WoundClot9Core Scientific Creation, Ltd.20160
K112800Suntouch Topical Hemostatic DressingHuizhou Foryou Medical Devices Co., Ltd.20120
K082601UltraClot, UltraClot OTCEmergency Medical Devices, LLC20080

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 12 years and passes through 3 companies; a new generation was cleared every 3.6 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K160679 (Core Scientific Creation, Ltd., 2016) has gone furthest, with 0 descendants of its own.
  • 5 other devices also cite its predicate K010933.

How does its category compare?

All QSY devices

QSY Hemostatic Wound Dressing Without Thrombin Or Other Biologics: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · QSY

2in 2025

2007: 132008: 72009: 92010: 72011: 82012: 72013: 32014: 62015: 62016: 52017: 12018: 52019: 42020: 12021: 12022: 22023: 72024: 42025: 22026 (partial year): 2
2007high 13 (2007) · low 1 (2017)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QSY

142in 2024

2007: 63 days median2008: 61 days median2009: 55 days median2010: 75 days median2011: 137 days median2012: 239 days median2013: 161 days median2014: 249 days median2015: 171 days median2016: 161 days median2018: 186 days median2019: 336 days median2023: 586 days median2024: 142 days median
2007high 586 (2023) · low 55 (2009)2026

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

Recalls per year · QSY

No recall names QSY since 2007.

Adverse event reports per year · QSY

14in 2025

2022: 12024: 32025: 14
2007high 14 (2025) · low 0 (2007)2025

MAUDE reports naming product code QSY, 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
2007136300
200876100
200995500
201077500
2011813700
2012723900
2013316100
2014624900
2015617100
2016516100
20171—00
2018518600
2019433600
20201—00
20211—00
20222—01
2023758600
2024414203
20252—014
20262—0—

What is it indicated for?

Topical control of bleeding from minor cuts and abrasions of the skin surface

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K071578: Bloodstop and Bloodstop IX Hemostatic Gauze, Models BS-10,BS-11,BS-12,B-13, BS-IX27, BS-IX-14, Bsix-15, Bsix-17.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K071578

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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