NOVOLINPEN DIAL-A-DOSE INSULIN DELIVERY SYSTEM
K-Number: K872805 · 1987-10-09
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Device Summary
Frequently Asked Questions
What is the NOVOLINPEN DIAL-A-DOSE INSULIN DELIVERY SYSTEM?
NOVOLINPEN DIAL-A-DOSE INSULIN DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Squibb-Novo, Inc.. The 510(k) number is K872805.
When did NOVOLINPEN DIAL-A-DOSE INSULIN DELIVERY SYSTEM receive FDA 510(k) clearance?
NOVOLINPEN DIAL-A-DOSE INSULIN DELIVERY SYSTEM received FDA 510(k) clearance on 1987-10-09, under 510(k) number K872805.
Who is the listed applicant for NOVOLINPEN DIAL-A-DOSE INSULIN DELIVERY SYSTEM?
The FDA 510(k) record lists Squibb-Novo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NOVOLINPEN DIAL-A-DOSE INSULIN DELIVERY SYSTEM?
The FDA product code for NOVOLINPEN DIAL-A-DOSE INSULIN DELIVERY SYSTEM is FMF.
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 Squibb-Novo, Inc. 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: FMF)
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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