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FDA 510(k)

MULTI-SNARE SET

K-Number: K011783 · 2002-01-24

ApplicantPfm Produkte Fur Die Medizin AG
Decision Date2002-01-24
Product CodeDXE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULTI-SNARE SET is the device name listed in this FDA 510(k) record. The listed applicant is Pfm Produkte Fur Die Medizin AG. It received FDA 510(k) clearance on 2002-01-24 under 510(k) number K011783. The device is classified under product code DXE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-SNARE SET?

MULTI-SNARE SET is a medical device that received FDA 510(k) clearance on 2002-01-24. The listed applicant is Pfm Produkte Fur Die Medizin AG. The 510(k) number is K011783.

When did MULTI-SNARE SET receive FDA 510(k) clearance?

MULTI-SNARE SET received FDA 510(k) clearance on 2002-01-24, under 510(k) number K011783.

Who is the listed applicant for MULTI-SNARE SET?

The FDA 510(k) record lists Pfm Produkte Fur Die Medizin AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI-SNARE SET?

The FDA product code for MULTI-SNARE SET is DXE.

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.

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Other records listing Pfm Produkte Fur Die Medizin AG 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.

K002471JETCAN HUBER NEEEDLE SETK001716REDON SET

Related Devices (Code: DXE)

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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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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