510(k) Report

510(k) · Cleared

Cleared

Premier Sterile Saline Wound Wash, Models 210 ML, WWM

K090848510(k) TraditionalCleared Jun 17, 200979-day reviewClass II21 CFR 880.5475

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

Premier Brands of America, Inc. · FQH Lavage, Jet

Cleared on Jun 17, 2009 as substantially equivalent to K083355 (Blairex Laboratories, Inc., 2008) and 2 other predicates after a 79-day review. Its family tree reaches back 6 generations to 1992. 1 later device descends from it.

Decided
Jun 17, 2009
Review
79 days
Class
Class II
Product code
FQH
Recalls
None
Predicates
3

Its longest line of descent runs back 6 generations to K914579 (1992). 38 ancestors in all, the oldest K890354 (1989). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 3 other ancestors2005: 2 other ancestors2007: 1 other ancestor2004: 3 other ancestors2001: 5 other ancestors2002: 2 other ancestors1999: 3 other ancestors1998: 3 other ancestors1997: 3 other ancestors1995: 2 other ancestors1994: 2 other ancestors1993: 1 other ancestor1989: 2 other ancestors2022: 1 descendant clearedK914579 · Silver Foam Wound Dressing · Vitaphore Corp. · 1992K955453 · Acticoat Silver Coated Dressing · Westaim Technologies, Inc. · 1996K981299 · Silverlon Contact Wound Dressing · Argentum International, LLC · 1998K023612 · Silverlon Contact Wound Dressing · Argentum International, LLC · 2003K063063 · Silvacide Skin & Wound Moisturizing Solution · Medical Molecular Therapuetics, LLC · 2007K083355 · Wound Wash Saline, 210 ML, Model B8552, Wound Wash Saline, 90 ML, Model B8553 · Blairex Laboratories, Inc. · 20081990200020102020
  1. Root · 6 generations backK914579 Silver Foam Wound DressingVitaphore Corp. · 1992
  2. 5 generations backK955453 Acticoat Silver Coated DressingWestaim Technologies, Inc. · 1996
  3. 4 generations backK981299 Silverlon Contact Wound DressingArgentum International, LLC · 1998
  4. 3 generations backK023612 Silverlon Contact Wound DressingArgentum International, LLC · 2003
  5. 2 generations backK063063 Silvacide Skin & Wound Moisturizing SolutionMedical Molecular Therapuetics, LLC · 2007
  6. 1 generation backK083355 Wound Wash Saline, 210 ML, Model B8552, Wound Wash Saline, 90 ML…Blairex Laboratories, Inc. · 2008
  7. This deviceK090848 Premier Sterile Saline Wound Wash, Models 210 ML, WWMPremier Brands of America, Inc. · 2009
  8. Descendant · cites it directly · 0 of its ownK210987 IRRIGO Wound Wash Jet SystemInopro, Inc. · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K210987IRRIGO Wound Wash Jet SystemInopro, Inc. · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K914579Silver Foam Wound DressingVitaphore Corp.1992—
−5K955453Acticoat Silver Coated DressingWestaim Technologies, Inc.1996—
−4K981299Silverlon Contact Wound DressingArgentum International, LLC1998—
−3K023612Silverlon Contact Wound DressingArgentum International, LLC2003—
−2K063063Silvacide Skin & Wound Moisturizing SolutionMedical Molecular Therapuetics, LLC2007—
−1K083355Wound Wash Saline, 210 ML, Model B8552, Wound Wash Saline, 90 ML, Model B8553Blairex Laboratories, Inc.2008—
0 (this device)K090848Premier Sterile Saline Wound Wash, Models 210 ML, WWMPremier Brands of America, Inc.2009—
+1K210987IRRIGO Wound Wash Jet SystemInopro, Inc.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198920
199310
199420
199520
199730
199830
199930
200150
200220
200430
200520
200710
200830

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K090848, 1992–2022Source: 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 FQH? 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 FQH device

  1. #1 K253996 BD Surgiphor™ Antimicrobial Irrigation System…score 14.8 · 14 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (3)

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
*K083355Wound Wash Saline, 210 ML, Model B8552, Wound Wash Saline, 90 ML, Model B8553
Summary page 2
…Wound Wash is an Rx and OTC device and will only be labeled for use in wounds. 6. Predicate Device OTC: Wound Wash Saline; Blairex Laboratories, Inc. (K083355) RX: Dermacyn TM Wound Dressing (K041161) Sterile Saline (K082330) 7. Intended Use/Indication for…
Blairex Laboratories, Inc.2008—
*K041161Microcyn Wound Care Dressing
Summary page 2
…abeled for use in wounds. 6. Predicate Device OTC: Wound Wash Saline; Blairex Laboratories, Inc. (K083355) RX: Dermacyn TM Wound Dressing (K041161) Sterile Saline (K082330) 7. Intended Use/Indication for Use Indications for Rx (Prescription)…
Oculus Innovative Sciences, Inc.20052
*K082330Primary Care Solutions, Inc., Sterile Water and Saline for Irrigation
Summary page 2
…Predicate Device OTC: Wound Wash Saline; Blairex Laboratories, Inc. (K083355) RX: Dermacyn TM Wound Dressing (K041161) Sterile Saline (K082330) 7. Intended Use/Indication for Use Indications for Rx (Prescription) Use: Saline Wound Wash…
Primary Care Solutions, Inc.2008—

Also cleared against K083355: 3 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K210987IRRIGO Wound Wash Jet SystemInopro, Inc.20220

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 17 years and passes through 6 companies; a new generation was cleared every 4.3 years on median.
  • 1 of the 38 ancestors has a recall of any class.
  • Of its descendants, K210987 (Inopro, Inc., 2022) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K083355.

How does its category compare?

All FQH devices

FQH Lavage, Jet: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · FQH

3in 2023

2007: 12009: 32011: 22012: 12015: 12016: 12020: 32021: 12022: 42023: 32026 (partial year): 2
2007high 4 (2022) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FQH

410in 2023

2009: 240 days median2020: 130 days median2022: 136 days median2023: 410 days median
2007high 410 (2023) · low 130 (2020)2026

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

Recalls per year · FQH

2in 2019

2007: 132009: 12010: 72017: 12019: 2
2007high 13 (2007) · low 0 (2008)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · FQH

835in 2025

2007: 102008: 272009: 702010: 1352011: 832012: 1332013: 1342014: 1942015: 1162016: 1502017: 2432018: 3172019: 3282020: 3932021: 3982022: 1712023: 3332024: 4252025: 835
2007high 835 (2025) · low 10 (2007)2025

MAUDE reports naming product code FQH, 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
20071—1310
20080—027
20093240170
20100—7135
20112—083
20121—0133
20130—0134
20140—0194
20151—0116
20161—0150
20170—1243
20180—0317
20190—2328
202031300393
20211—0398
202241360171
202334100333
20240—0425
20250—0835
20262—0—

What is it indicated for?

Saline Wound Wash is intended for use by or under the direction of a professional health care provider in moistening and lubricating absorbent wound dressings, cleansing and maintaining a moist wound environment for traumatic wounds such as pressure sores, leg ulcers of diabetic and vascular origin, cuts abrasions and minor bums.

Saline Wound Wash is intended for use in moistening and lubricating absorbent wound dressings and for cleansing minor wounds, scrapes and minor bums. If redness, swelling or bleeding continues please seek the help of a nurse, nurses aid, doctor or other medical professional.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K090848: Premier Sterile Saline Wound Wash, Models 210 ML, WWM.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K090848

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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