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FDA 510(k)

PHACOTRON SYSTEMS PLUS III PHACOEMULSIFIER ASPI.

K-Number: K902876 · 1990-09-18

ApplicantIntraoptics Surgical, Inc.
Decision Date1990-09-18
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PHACOTRON SYSTEMS PLUS III PHACOEMULSIFIER ASPI. is the device name listed in this FDA 510(k) record. The listed applicant is Intraoptics Surgical, Inc.. It received FDA 510(k) clearance on 1990-09-18 under 510(k) number K902876. 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 PHACOTRON SYSTEMS PLUS III PHACOEMULSIFIER ASPI.?

PHACOTRON SYSTEMS PLUS III PHACOEMULSIFIER ASPI. is a medical device that received FDA 510(k) clearance on 1990-09-18. The listed applicant is Intraoptics Surgical, Inc.. The 510(k) number is K902876.

When did PHACOTRON SYSTEMS PLUS III PHACOEMULSIFIER ASPI. receive FDA 510(k) clearance?

PHACOTRON SYSTEMS PLUS III PHACOEMULSIFIER ASPI. received FDA 510(k) clearance on 1990-09-18, under 510(k) number K902876.

Who is the listed applicant for PHACOTRON SYSTEMS PLUS III PHACOEMULSIFIER ASPI.?

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

What is the FDA product code for PHACOTRON SYSTEMS PLUS III PHACOEMULSIFIER ASPI.?

The FDA product code for PHACOTRON SYSTEMS PLUS III PHACOEMULSIFIER ASPI. is HQC.

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Related Devices (Code: HQC)

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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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