INPERSOL-CAPD ADMINISTRATION SET
K-Number: K801881 · 1980-10-10
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Device Summary
Frequently Asked Questions
What is the INPERSOL-CAPD ADMINISTRATION SET?
INPERSOL-CAPD ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Abbott Laboratories. The 510(k) number is K801881.
When did INPERSOL-CAPD ADMINISTRATION SET receive FDA 510(k) clearance?
INPERSOL-CAPD ADMINISTRATION SET received FDA 510(k) clearance on 1980-10-10, under 510(k) number K801881.
Who is the listed applicant for INPERSOL-CAPD ADMINISTRATION SET?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INPERSOL-CAPD ADMINISTRATION SET?
The FDA product code for INPERSOL-CAPD ADMINISTRATION SET is KDJ.
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 Abbott Laboratories 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: KDJ)
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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