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FDA 510(k)

OPHTHALMIC FITLER MICRO CAPSULE

K-Number: K863729 · 1986-10-10

ApplicantIpax, Inc.
Decision Date1986-10-10
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTHALMIC FITLER MICRO CAPSULE is the device name listed in this FDA 510(k) record. The listed applicant is Ipax, Inc.. It received FDA 510(k) clearance on 1986-10-10 under 510(k) number K863729. 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 OPHTHALMIC FITLER MICRO CAPSULE?

OPHTHALMIC FITLER MICRO CAPSULE is a medical device that received FDA 510(k) clearance on 1986-10-10. The listed applicant is Ipax, Inc.. The 510(k) number is K863729.

When did OPHTHALMIC FITLER MICRO CAPSULE receive FDA 510(k) clearance?

OPHTHALMIC FITLER MICRO CAPSULE received FDA 510(k) clearance on 1986-10-10, under 510(k) number K863729.

Who is the listed applicant for OPHTHALMIC FITLER MICRO CAPSULE?

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

What is the FDA product code for OPHTHALMIC FITLER MICRO CAPSULE?

The FDA product code for OPHTHALMIC FITLER MICRO CAPSULE is HQC.

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Related Devices (Code: HQC)

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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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