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FDA 510(k)

ECOMED SCALP VEIN SET

K-Number: K992145 · 1999-10-14

Decision Date1999-10-14
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ECOMED SCALP VEIN SET is the device name listed in this FDA 510(k) record. The listed applicant is Greiner Meditech, Inc.. It received FDA 510(k) clearance on 1999-10-14 under 510(k) number K992145. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECOMED SCALP VEIN SET?

ECOMED SCALP VEIN SET is a medical device that received FDA 510(k) clearance on 1999-10-14. The listed applicant is Greiner Meditech, Inc.. The 510(k) number is K992145.

When did ECOMED SCALP VEIN SET receive FDA 510(k) clearance?

ECOMED SCALP VEIN SET received FDA 510(k) clearance on 1999-10-14, under 510(k) number K992145.

Who is the listed applicant for ECOMED SCALP VEIN SET?

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

What is the FDA product code for ECOMED SCALP VEIN SET?

The FDA product code for ECOMED SCALP VEIN SET is FPA.

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 Greiner Meditech, 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.

View all 10 devices →

Related Devices (Code: FPA)

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

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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