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FDA 510(k)

OPHTHALMIC SPONGES

K-Number: K950241 · 1995-02-27

ApplicantOasis Medical, Inc.
Decision Date1995-02-27
Product CodeHOZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTHALMIC SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Oasis Medical, Inc.. It received FDA 510(k) clearance on 1995-02-27 under 510(k) number K950241. The device is classified under product code HOZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPHTHALMIC SPONGES?

OPHTHALMIC SPONGES is a medical device that received FDA 510(k) clearance on 1995-02-27. The listed applicant is Oasis Medical, Inc.. The 510(k) number is K950241.

When did OPHTHALMIC SPONGES receive FDA 510(k) clearance?

OPHTHALMIC SPONGES received FDA 510(k) clearance on 1995-02-27, under 510(k) number K950241.

Who is the listed applicant for OPHTHALMIC SPONGES?

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

What is the FDA product code for OPHTHALMIC SPONGES?

The FDA product code for OPHTHALMIC SPONGES is HOZ.

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Other records listing Oasis Medical, Inc. as applicant

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Related Devices (Code: HOZ)

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

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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