FLO-RESTER
K-Number: K883696 · 1988-11-30
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Device Summary
Frequently Asked Questions
What is the FLO-RESTER?
FLO-RESTER is a medical device that received FDA 510(k) clearance on 1988-11-30. The listed applicant is Bio-Vascular, Inc.. The 510(k) number is K883696.
When did FLO-RESTER receive FDA 510(k) clearance?
FLO-RESTER received FDA 510(k) clearance on 1988-11-30, under 510(k) number K883696.
Who is the listed applicant for FLO-RESTER?
The FDA 510(k) record lists Bio-Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLO-RESTER?
The FDA product code for FLO-RESTER is DXC.
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 Bio-Vascular, 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: DXC)
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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