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FDA 510(k)

VISITEC ASPIRATING SYRINGE

K-Number: K923645 · 1992-09-30

ApplicantVisitec Co.
Decision Date1992-09-30
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VISITEC ASPIRATING SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Visitec Co.. It received FDA 510(k) clearance on 1992-09-30 under 510(k) number K923645. 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 VISITEC ASPIRATING SYRINGE?

VISITEC ASPIRATING SYRINGE is a medical device that received FDA 510(k) clearance on 1992-09-30. The listed applicant is Visitec Co.. The 510(k) number is K923645.

When did VISITEC ASPIRATING SYRINGE receive FDA 510(k) clearance?

VISITEC ASPIRATING SYRINGE received FDA 510(k) clearance on 1992-09-30, under 510(k) number K923645.

Who is the listed applicant for VISITEC ASPIRATING SYRINGE?

The FDA 510(k) record lists Visitec Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VISITEC ASPIRATING SYRINGE?

The FDA product code for VISITEC ASPIRATING 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 Visitec Co. 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.

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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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