FLORET STRUNG GAUZE SPONGES
K-Number: K830261 · 1983-06-08
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Device Summary
Frequently Asked Questions
What is the FLORET STRUNG GAUZE SPONGES?
FLORET STRUNG GAUZE SPONGES is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Ritmed, Inc.. The 510(k) number is K830261.
When did FLORET STRUNG GAUZE SPONGES receive FDA 510(k) clearance?
FLORET STRUNG GAUZE SPONGES received FDA 510(k) clearance on 1983-06-08, under 510(k) number K830261.
Who is the listed applicant for FLORET STRUNG GAUZE SPONGES?
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 STRUNG GAUZE SPONGES?
The FDA product code for FLORET STRUNG GAUZE SPONGES 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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