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FDA 510(k)

CPD COMMANDER

K-Number: K974253 · 1998-02-25

ApplicantScieran Technologies, Inc.
Decision Date1998-02-25
Product CodeMRH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CPD 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 1998-02-25 under 510(k) number K974253. The device is classified under product code MRH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPD COMMANDER?

CPD COMMANDER is a medical device that received FDA 510(k) clearance on 1998-02-25. The listed applicant is Scieran Technologies, Inc.. The 510(k) number is K974253.

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

CPD COMMANDER received FDA 510(k) clearance on 1998-02-25, under 510(k) number K974253.

Who is the listed applicant for CPD 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 CPD COMMANDER?

The FDA product code for CPD COMMANDER is MRH.

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.

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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.

K980085PHACO COMMANDERK973749FRAG COMMANDERK961738VIT COMMANDER SYSTEMK960767LIGHT COMMANDER

Related Devices (Code: MRH)

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.

K253760OMNI Ultra Surgical System (1-110)Sight Sciences, Inc.K243503VIA360™ Surgical SystemNew World Medical, Inc.K232214OMNI Surgical SystemSight Sciences, Inc.K213173TrabEx ProMicrosurgical Technologies, Inc.K212797iPrime Viscodelivery SystemGlaukosK211680Streamline Surgical SystemNew World Medical, Inc.

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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