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FDA 510(k)

IODOFORM PACKAGING STRIP

K-Number: K940339 · 1994-02-25

ApplicantAlbahealth Products
Decision Date1994-02-25
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

IODOFORM PACKAGING STRIP is the device name listed in this FDA 510(k) record. The listed applicant is Albahealth Products. It received FDA 510(k) clearance on 1994-02-25 under 510(k) number K940339. 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 IODOFORM PACKAGING STRIP?

IODOFORM PACKAGING STRIP is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Albahealth Products. The 510(k) number is K940339.

When did IODOFORM PACKAGING STRIP receive FDA 510(k) clearance?

IODOFORM PACKAGING STRIP received FDA 510(k) clearance on 1994-02-25, under 510(k) number K940339.

Who is the listed applicant for IODOFORM PACKAGING STRIP?

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

What is the FDA product code for IODOFORM PACKAGING STRIP?

The FDA product code for IODOFORM PACKAGING STRIP is FRO. This falls under the Anesthesiology category.

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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.

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Official Source

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

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