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FDA 510(k)

TITANIUM SUCTION TIP

K-Number: K874401 · 1987-11-12

Decision Date1987-11-12
Product CodeEHZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TITANIUM SUCTION TIP is the device name listed in this FDA 510(k) record. The listed applicant is Implant Innovations International, Inc.. It received FDA 510(k) clearance on 1987-11-12 under 510(k) number K874401. The device is classified under product code EHZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITANIUM SUCTION TIP?

TITANIUM SUCTION TIP is a medical device that received FDA 510(k) clearance on 1987-11-12. The listed applicant is Implant Innovations International, Inc.. The 510(k) number is K874401.

When did TITANIUM SUCTION TIP receive FDA 510(k) clearance?

TITANIUM SUCTION TIP received FDA 510(k) clearance on 1987-11-12, under 510(k) number K874401.

Who is the listed applicant for TITANIUM SUCTION TIP?

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

What is the FDA product code for TITANIUM SUCTION TIP?

The FDA product code for TITANIUM SUCTION TIP is EHZ.

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 Implant Innovations International, 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 18 devices →

Related Devices (Code: EHZ)

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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