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FDA 510(k)

SUCRALFATE AND CARAFATE PASTE KITS

K-Number: K043587 · 2006-02-03

ApplicantPatrick D. Mcgrath Ph.D
Decision Date2006-02-03
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

SUCRALFATE AND CARAFATE PASTE KITS is the device name listed in this FDA 510(k) record. The listed applicant is Patrick D. Mcgrath Ph.D. It received FDA 510(k) clearance on 2006-02-03 under 510(k) number K043587. 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 SUCRALFATE AND CARAFATE PASTE KITS?

SUCRALFATE AND CARAFATE PASTE KITS is a medical device that received FDA 510(k) clearance on 2006-02-03. The listed applicant is Patrick D. Mcgrath Ph.D. The 510(k) number is K043587.

When did SUCRALFATE AND CARAFATE PASTE KITS receive FDA 510(k) clearance?

SUCRALFATE AND CARAFATE PASTE KITS received FDA 510(k) clearance on 2006-02-03, under 510(k) number K043587.

Who is the listed applicant for SUCRALFATE AND CARAFATE PASTE KITS?

The FDA 510(k) record lists Patrick D. Mcgrath Ph.D as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCRALFATE AND CARAFATE PASTE KITS?

The FDA product code for SUCRALFATE AND CARAFATE PASTE KITS is FRO. This falls under the Anesthesiology category.

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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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