Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MEDLINE IODOFORM PACKING STRIPS

K-Number: K052720 · 2005-10-20

Decision Date2005-10-20
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

MEDLINE IODOFORM PACKING STRIPS is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2005-10-20 under 510(k) number K052720. 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 MEDLINE IODOFORM PACKING STRIPS?

MEDLINE IODOFORM PACKING STRIPS is a medical device that received FDA 510(k) clearance on 2005-10-20. The listed applicant is Medline Industries, Inc.. The 510(k) number is K052720.

When did MEDLINE IODOFORM PACKING STRIPS receive FDA 510(k) clearance?

MEDLINE IODOFORM PACKING STRIPS received FDA 510(k) clearance on 2005-10-20, under 510(k) number K052720.

Who is the listed applicant for MEDLINE IODOFORM PACKING STRIPS?

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

What is the FDA product code for MEDLINE IODOFORM PACKING STRIPS?

The FDA product code for MEDLINE IODOFORM PACKING STRIPS 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.

Other records listing Medline Industries, 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.

View all 223 devices →

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.

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.

↑