BIOSPAL 3000 S
K-Number: K832645 · 1983-09-20
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Device Summary
Frequently Asked Questions
What is the BIOSPAL 3000 S?
BIOSPAL 3000 S is a medical device that received FDA 510(k) clearance on 1983-09-20. The listed applicant is Hospal Medical Corp.. The 510(k) number is K832645.
When did BIOSPAL 3000 S receive FDA 510(k) clearance?
BIOSPAL 3000 S received FDA 510(k) clearance on 1983-09-20, under 510(k) number K832645.
Who is the listed applicant for BIOSPAL 3000 S?
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 3000 S?
The FDA product code for BIOSPAL 3000 S is KDI.
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: KDI)
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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