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FDA 510(k)

PHYSICIAN INDUSTRIES' DURAMETER SYRINGE

K-Number: K033739 · 2004-07-12

Decision Date2004-07-12
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PHYSICIAN INDUSTRIES' DURAMETER SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Physician Industries, Inc.. It received FDA 510(k) clearance on 2004-07-12 under 510(k) number K033739. 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 PHYSICIAN INDUSTRIES' DURAMETER SYRINGE?

PHYSICIAN INDUSTRIES' DURAMETER SYRINGE is a medical device that received FDA 510(k) clearance on 2004-07-12. The listed applicant is Physician Industries, Inc.. The 510(k) number is K033739.

When did PHYSICIAN INDUSTRIES' DURAMETER SYRINGE receive FDA 510(k) clearance?

PHYSICIAN INDUSTRIES' DURAMETER SYRINGE received FDA 510(k) clearance on 2004-07-12, under 510(k) number K033739.

Who is the listed applicant for PHYSICIAN INDUSTRIES' DURAMETER SYRINGE?

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

What is the FDA product code for PHYSICIAN INDUSTRIES' DURAMETER SYRINGE?

The FDA product code for PHYSICIAN INDUSTRIES' DURAMETER 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 Physician Industries, 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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