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FDA 510(k)

FUTURA TOPCAP NON GAMMA-2

K-Number: K011801 · 2001-08-16

ApplicantAb Ardent
Decision Date2001-08-16
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FUTURA TOPCAP NON GAMMA-2 is the device name listed in this FDA 510(k) record. The listed applicant is Ab Ardent. It received FDA 510(k) clearance on 2001-08-16 under 510(k) number K011801. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUTURA TOPCAP NON GAMMA-2?

FUTURA TOPCAP NON GAMMA-2 is a medical device that received FDA 510(k) clearance on 2001-08-16. The listed applicant is Ab Ardent. The 510(k) number is K011801.

When did FUTURA TOPCAP NON GAMMA-2 receive FDA 510(k) clearance?

FUTURA TOPCAP NON GAMMA-2 received FDA 510(k) clearance on 2001-08-16, under 510(k) number K011801.

Who is the listed applicant for FUTURA TOPCAP NON GAMMA-2?

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

What is the FDA product code for FUTURA TOPCAP NON GAMMA-2?

The FDA product code for FUTURA TOPCAP NON GAMMA-2 is EJJ.

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 Ab Ardent 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 13 devices →

Related Devices (Code: EJJ)

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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