FLORET GAUZE PACKING
K-Number: K830278 · 1983-03-29
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Device Summary
Frequently Asked Questions
What is the FLORET GAUZE PACKING?
FLORET GAUZE PACKING is a medical device that received FDA 510(k) clearance on 1983-03-29. The listed applicant is Ritmed, Inc.. The 510(k) number is K830278.
When did FLORET GAUZE PACKING receive FDA 510(k) clearance?
FLORET GAUZE PACKING received FDA 510(k) clearance on 1983-03-29, under 510(k) number K830278.
Who is the listed applicant for FLORET GAUZE PACKING?
The FDA 510(k) record lists Ritmed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLORET GAUZE PACKING?
The FDA product code for FLORET GAUZE PACKING is EFQ.
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 Ritmed, 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.
Related Devices (Code: EFQ)
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.
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