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FDA 510(k)

INFINITECH LIGHTED INFUSION CANNULA

K-Number: K946136 · 1995-10-02

ApplicantSurgical Technologies, Inc.
Decision Date1995-10-02
Product CodeMPA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INFINITECH LIGHTED INFUSION CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Technologies, Inc.. It received FDA 510(k) clearance on 1995-10-02 under 510(k) number K946136. The device is classified under product code MPA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFINITECH LIGHTED INFUSION CANNULA?

INFINITECH LIGHTED INFUSION CANNULA is a medical device that received FDA 510(k) clearance on 1995-10-02. The listed applicant is Surgical Technologies, Inc.. The 510(k) number is K946136.

When did INFINITECH LIGHTED INFUSION CANNULA receive FDA 510(k) clearance?

INFINITECH LIGHTED INFUSION CANNULA received FDA 510(k) clearance on 1995-10-02, under 510(k) number K946136.

Who is the listed applicant for INFINITECH LIGHTED INFUSION CANNULA?

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

What is the FDA product code for INFINITECH LIGHTED INFUSION CANNULA?

The FDA product code for INFINITECH LIGHTED INFUSION CANNULA is MPA.

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Other records listing Surgical Technologies, 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.

K941992CYSTOSCOPEK942029ARTHROSCOPEK952566OSCILFLATORK951918SURGICAL TECHNOLOGIES, INC. SYRINGEK950683ARTHROGRAM TRAYK946135INFINITECH ASPIRATING LASER PROBE

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Related Devices (Code: MPA)

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.

K253468Nova Eye iTrack™ 250A Canaloplasty Microcatheter (iTrack™ 250A)Nova Eye, Inc.K242184Alcon 27GA Chandelier (8065000252); Alcon 27+ DS Wide Angle Endoilluminator (8065000253); Alcon 27+ DS Endoilluminator (8065000256);Alcon Laboratories, Inc.K233653Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga (3269.M04-00)Peregrine Surgical, LLCK221872ITrack Advance Canaloplasty Microcatheter with Advanced Delivery SystemNova Eye Inc. (Business Name Nova Eye Medical)K202670Nam illumination probe with chopperOculight , Ltd.K080067ISCIENCE INTERVENTIONAL OPHTHALMIC MICROCATHETERIscience Interventional

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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