FDA 510(k)

OPHTHALAS DYE OPHTHALMIC LASER

K-Number: K873460 · 1987-10-29

Decision Date1987-10-29

Product CodeHQF

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

OPHTHALAS DYE OPHTHALMIC LASER is the device name listed in this FDA 510(k) record. The listed applicant is Biophysic Medical, Inc.. It received FDA 510(k) clearance on 1987-10-29 under 510(k) number K873460. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPHTHALAS DYE OPHTHALMIC LASER?

OPHTHALAS DYE OPHTHALMIC LASER is a medical device that received FDA 510(k) clearance on 1987-10-29. The listed applicant is Biophysic Medical, Inc.. The 510(k) number is K873460.

When did OPHTHALAS DYE OPHTHALMIC LASER receive FDA 510(k) clearance?

OPHTHALAS DYE OPHTHALMIC LASER received FDA 510(k) clearance on 1987-10-29, under 510(k) number K873460.

Who is the listed applicant for OPHTHALAS DYE OPHTHALMIC LASER?

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

What is the FDA product code for OPHTHALAS DYE OPHTHALMIC LASER?

The FDA product code for OPHTHALAS DYE OPHTHALMIC LASER is HQF.

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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.