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FDA 510(k)

DISPOSABLE SYRINGE

K-Number: K841578 · 1984-05-07

Decision Date1984-05-07
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Ava Medical Products of Canada, Inc.. It received FDA 510(k) clearance on 1984-05-07 under 510(k) number K841578. 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 DISPOSABLE SYRINGE?

DISPOSABLE SYRINGE is a medical device that received FDA 510(k) clearance on 1984-05-07. The listed applicant is Ava Medical Products of Canada, Inc.. The 510(k) number is K841578.

When did DISPOSABLE SYRINGE receive FDA 510(k) clearance?

DISPOSABLE SYRINGE received FDA 510(k) clearance on 1984-05-07, under 510(k) number K841578.

Who is the listed applicant for DISPOSABLE SYRINGE?

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

What is the FDA product code for DISPOSABLE SYRINGE?

The FDA product code for DISPOSABLE SYRINGE 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 Ava Medical Products of Canada, 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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