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FDA 510(k)

SALINE WET DRESSING- STERILE

K-Number: K934258 · 1993-11-24

ApplicantTrinity Laboratories, Inc.
Decision Date1993-11-24
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

SALINE WET DRESSING- STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Trinity Laboratories, Inc.. It received FDA 510(k) clearance on 1993-11-24 under 510(k) number K934258. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALINE WET DRESSING- STERILE?

SALINE WET DRESSING- STERILE is a medical device that received FDA 510(k) clearance on 1993-11-24. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K934258.

When did SALINE WET DRESSING- STERILE receive FDA 510(k) clearance?

SALINE WET DRESSING- STERILE received FDA 510(k) clearance on 1993-11-24, under 510(k) number K934258.

Who is the listed applicant for SALINE WET DRESSING- STERILE?

The FDA 510(k) record lists Trinity Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SALINE WET DRESSING- STERILE?

The FDA product code for SALINE WET DRESSING- STERILE is FRO. This falls under the Anesthesiology category.

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Other records listing Trinity Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K981441HEART CATH TRAY, STERILE, DISPOSABLEK974238DENTAL TRAY, STERILE, DISPOSABLEK974286CIRCUMCISION TRAY, CAT. NO. 70340K972160CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE AGGLUTNATION LATEX TESTK970722EYE TRAYK965201O.R. SCRUB PREP TRAY, STERILE, DISPOSABLE

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Related Devices (Code: FRO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254168Actolind® (06.3637. Actolind® Gel Plus)ACTO GmbHK254041SkinSmart Antimicrobial HydroGelMagic Science Supply, LLCK261646Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd.K253665Vashe Plus Antimicrobial SolutionUrgo Medical North America, LLCK251929SilverCeuticals® Antimicrobial Wound GelSilverceuticals, Inc.K261023Microdacyn Wound Irrigation SolutionSonoma Pharmaceuticals, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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