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FDA 510(k)

FIRST AID KIT

K-Number: K830373 · 1983-05-13

ApplicantAkla, Inc.
Decision Date1983-05-13
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

FIRST AID KIT is the device name listed in this FDA 510(k) record. The listed applicant is Akla, Inc.. It received FDA 510(k) clearance on 1983-05-13 under 510(k) number K830373. 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 FIRST AID KIT?

FIRST AID KIT is a medical device that received FDA 510(k) clearance on 1983-05-13. The listed applicant is Akla, Inc.. The 510(k) number is K830373.

When did FIRST AID KIT receive FDA 510(k) clearance?

FIRST AID KIT received FDA 510(k) clearance on 1983-05-13, under 510(k) number K830373.

Who is the listed applicant for FIRST AID KIT?

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

What is the FDA product code for FIRST AID KIT?

The FDA product code for FIRST AID KIT is FRO. This falls under the Anesthesiology category.

Related Clinical Trials

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.

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Other records listing Akla, 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.

K830375FIRST AID BAGS #1,2,3K830374RESCUE PACK

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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