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FDA 510(k)

STERIPACK STERILE DISPOSABLE SYRINGE & STERILE DISPOSABLE INSULIN SYRINGE

K-Number: K023108 · 2002-12-03

ApplicantAtlantic Products, Inc.
Decision Date2002-12-03
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERIPACK STERILE DISPOSABLE SYRINGE & STERILE DISPOSABLE INSULIN SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Atlantic Products, Inc.. It received FDA 510(k) clearance on 2002-12-03 under 510(k) number K023108. 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 STERIPACK STERILE DISPOSABLE SYRINGE & STERILE DISPOSABLE INSULIN SYRINGE?

STERIPACK STERILE DISPOSABLE SYRINGE & STERILE DISPOSABLE INSULIN SYRINGE is a medical device that received FDA 510(k) clearance on 2002-12-03. The listed applicant is Atlantic Products, Inc.. The 510(k) number is K023108.

When did STERIPACK STERILE DISPOSABLE SYRINGE & STERILE DISPOSABLE INSULIN SYRINGE receive FDA 510(k) clearance?

STERIPACK STERILE DISPOSABLE SYRINGE & STERILE DISPOSABLE INSULIN SYRINGE received FDA 510(k) clearance on 2002-12-03, under 510(k) number K023108.

Who is the listed applicant for STERIPACK STERILE DISPOSABLE SYRINGE & STERILE DISPOSABLE INSULIN SYRINGE?

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

What is the FDA product code for STERIPACK STERILE DISPOSABLE SYRINGE & STERILE DISPOSABLE INSULIN SYRINGE?

The FDA product code for STERIPACK STERILE DISPOSABLE SYRINGE & STERILE DISPOSABLE INSULIN SYRINGE is FMF.

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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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