DISSCAP 110
K-Number: K820966 · 1982-04-16
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Device Summary
Frequently Asked Questions
What is the DISSCAP 110?
DISSCAP 110 is a medical device that received FDA 510(k) clearance on 1982-04-16. The listed applicant is Hospal Medical Corp.. The 510(k) number is K820966.
When did DISSCAP 110 receive FDA 510(k) clearance?
DISSCAP 110 received FDA 510(k) clearance on 1982-04-16, under 510(k) number K820966.
Who is the listed applicant for DISSCAP 110?
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 110?
The FDA product code for DISSCAP 110 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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