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FDA 510(k)

PHACO COMMANDER

K-Number: K980085 · 1998-02-24

ApplicantScieran Technologies, Inc.
Decision Date1998-02-24
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PHACO COMMANDER is the device name listed in this FDA 510(k) record. The listed applicant is Scieran Technologies, Inc.. It received FDA 510(k) clearance on 1998-02-24 under 510(k) number K980085. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHACO COMMANDER?

PHACO COMMANDER is a medical device that received FDA 510(k) clearance on 1998-02-24. The listed applicant is Scieran Technologies, Inc.. The 510(k) number is K980085.

When did PHACO COMMANDER receive FDA 510(k) clearance?

PHACO COMMANDER received FDA 510(k) clearance on 1998-02-24, under 510(k) number K980085.

Who is the listed applicant for PHACO COMMANDER?

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

What is the FDA product code for PHACO COMMANDER?

The FDA product code for PHACO COMMANDER is HQC.

Related Clinical Trials

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Other records listing Scieran 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.

K974253CPD COMMANDERK973749FRAG COMMANDERK961738VIT COMMANDER SYSTEMK960767LIGHT COMMANDER

Related Devices (Code: HQC)

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

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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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