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FDA 510(k)

SIMPLICITY SOFT QD MICRO INFUSION SET

K-Number: K012845 · 2001-09-14

Decision Date2001-09-14
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SIMPLICITY SOFT QD MICRO INFUSION SET is the device name listed in this FDA 510(k) record. The listed applicant is Sterling Medivations, Inc.. It received FDA 510(k) clearance on 2001-09-14 under 510(k) number K012845. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMPLICITY SOFT QD MICRO INFUSION SET?

SIMPLICITY SOFT QD MICRO INFUSION SET is a medical device that received FDA 510(k) clearance on 2001-09-14. The listed applicant is Sterling Medivations, Inc.. The 510(k) number is K012845.

When did SIMPLICITY SOFT QD MICRO INFUSION SET receive FDA 510(k) clearance?

SIMPLICITY SOFT QD MICRO INFUSION SET received FDA 510(k) clearance on 2001-09-14, under 510(k) number K012845.

Who is the listed applicant for SIMPLICITY SOFT QD MICRO INFUSION SET?

The FDA 510(k) record lists Sterling Medivations, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIMPLICITY SOFT QD MICRO INFUSION SET?

The FDA product code for SIMPLICITY SOFT QD MICRO INFUSION SET is FPA.

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 Sterling Medivations, 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.

View all 27 devices →

Related Devices (Code: FPA)

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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