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FDA 510(k)

MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER

K-Number: K000438 · 2000-05-03

Decision Date2000-05-03
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Biosurgical Corp.. It received FDA 510(k) clearance on 2000-05-03 under 510(k) number K000438. 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 MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER?

MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER is a medical device that received FDA 510(k) clearance on 2000-05-03. The listed applicant is Biosurgical Corp.. The 510(k) number is K000438.

When did MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER receive FDA 510(k) clearance?

MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER received FDA 510(k) clearance on 2000-05-03, under 510(k) number K000438.

Who is the listed applicant for MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER?

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

What is the FDA product code for MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER?

The FDA product code for MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER 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 Biosurgical Corp. 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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