MULTISKAN (78-503-00)
K-Number: K790422 · 1979-04-20
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Device Summary
Frequently Asked Questions
What is the MULTISKAN (78-503-00)?
MULTISKAN (78-503-00) is a medical device that received FDA 510(k) clearance on 1979-04-20. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K790422.
When did MULTISKAN (78-503-00) receive FDA 510(k) clearance?
MULTISKAN (78-503-00) received FDA 510(k) clearance on 1979-04-20, under 510(k) number K790422.
Who is the listed applicant for MULTISKAN (78-503-00)?
The FDA 510(k) record lists Flow Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTISKAN (78-503-00)?
The FDA product code for MULTISKAN (78-503-00) is JJQ.
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 Flow 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: JJQ)
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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