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FDA 510(k)

BARD ABSORPTION DRESSING

K-Number: K831710 · 1984-01-03

Decision Date1984-01-03
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

BARD ABSORPTION DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K831710. 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 BARD ABSORPTION DRESSING?

BARD ABSORPTION DRESSING is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K831710.

When did BARD ABSORPTION DRESSING receive FDA 510(k) clearance?

BARD ABSORPTION DRESSING received FDA 510(k) clearance on 1984-01-03, under 510(k) number K831710.

Who is the listed applicant for BARD ABSORPTION DRESSING?

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

What is the FDA product code for BARD ABSORPTION DRESSING?

The FDA product code for BARD ABSORPTION DRESSING 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 C.R. Bard, 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.

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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.

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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