DISSCAP 080
K-Number: K822851 · 1982-10-04
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Device Summary
Frequently Asked Questions
What is the DISSCAP 080?
DISSCAP 080 is a medical device that received FDA 510(k) clearance on 1982-10-04. The listed applicant is Hospal Medical Corp.. The 510(k) number is K822851.
When did DISSCAP 080 receive FDA 510(k) clearance?
DISSCAP 080 received FDA 510(k) clearance on 1982-10-04, under 510(k) number K822851.
Who is the listed applicant for DISSCAP 080?
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 DISSCAP 080?
The FDA product code for DISSCAP 080 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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