BIOSPAL 2400S
K-Number: K840812 · 1984-04-02
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Device Summary
Frequently Asked Questions
What is the BIOSPAL 2400S?
BIOSPAL 2400S is a medical device that received FDA 510(k) clearance on 1984-04-02. The listed applicant is Hospal Medical Corp.. The 510(k) number is K840812.
When did BIOSPAL 2400S receive FDA 510(k) clearance?
BIOSPAL 2400S received FDA 510(k) clearance on 1984-04-02, under 510(k) number K840812.
Who is the listed applicant for BIOSPAL 2400S?
The FDA 510(k) record lists Hospal Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOSPAL 2400S?
The FDA product code for BIOSPAL 2400S is FKQ.
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 Hospal Medical Corp. 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: FKQ)
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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