SF CELLS
K-Number: K831683 · 1983-07-06
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Device Summary
Frequently Asked Questions
What is the SF CELLS?
SF CELLS is a medical device that received FDA 510(k) clearance on 1983-07-06. The listed applicant is Viromed Laboratories, Inc.. The 510(k) number is K831683.
When did SF CELLS receive FDA 510(k) clearance?
SF CELLS received FDA 510(k) clearance on 1983-07-06, under 510(k) number K831683.
Who is the listed applicant for SF CELLS?
The FDA 510(k) record lists Viromed Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SF CELLS?
The FDA product code for SF CELLS is KIR.
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 Viromed Laboratories, 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: KIR)
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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