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FDA 510(k)

NOVOLINPEN DIAL-A-DOSE INSULIN DELIVERY SYSTEM

K-Number: K872805 · 1987-10-09

Decision Date1987-10-09
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NOVOLINPEN DIAL-A-DOSE INSULIN DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Squibb-Novo, Inc.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K872805. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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