ROYCO MODEL 951 CELL MIXER
K-Number: K800104 · 1980-02-06
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Device Summary
Frequently Asked Questions
What is the ROYCO MODEL 951 CELL MIXER?
ROYCO MODEL 951 CELL MIXER is a medical device that received FDA 510(k) clearance on 1980-02-06. The listed applicant is Royco Instruments. The 510(k) number is K800104.
When did ROYCO MODEL 951 CELL MIXER receive FDA 510(k) clearance?
ROYCO MODEL 951 CELL MIXER received FDA 510(k) clearance on 1980-02-06, under 510(k) number K800104.
Who is the listed applicant for ROYCO MODEL 951 CELL MIXER?
The FDA 510(k) record lists Royco Instruments as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROYCO MODEL 951 CELL MIXER?
The FDA product code for ROYCO MODEL 951 CELL MIXER is KSQ.
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 Royco Instruments 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: KSQ)
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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