FLORET TONSIL & ADENOID SPONGES
K-Number: K830264 · 1983-06-03
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Device Summary
Frequently Asked Questions
What is the FLORET TONSIL & ADENOID SPONGES?
FLORET TONSIL & ADENOID SPONGES is a medical device that received FDA 510(k) clearance on 1983-06-03. The listed applicant is Ritmed, Inc.. The 510(k) number is K830264.
When did FLORET TONSIL & ADENOID SPONGES receive FDA 510(k) clearance?
FLORET TONSIL & ADENOID SPONGES received FDA 510(k) clearance on 1983-06-03, under 510(k) number K830264.
Who is the listed applicant for FLORET TONSIL & ADENOID 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 TONSIL & ADENOID SPONGES?
The FDA product code for FLORET TONSIL & ADENOID 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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