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FDA 510(k)

MSP OPHTHALMIC (EYE SPUD)

K-Number: K931449 · 1993-08-31

ApplicantMedical Sterile Products, Inc.
Decision Date1993-08-31
Product CodeHNA
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MSP OPHTHALMIC (EYE SPUD) is the device name listed in this FDA 510(k) record. The listed applicant is Medical Sterile Products, Inc.. It received FDA 510(k) clearance on 1993-08-31 under 510(k) number K931449. The device is classified under product code HNA. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSP OPHTHALMIC (EYE SPUD)?

MSP OPHTHALMIC (EYE SPUD) is a medical device that received FDA 510(k) clearance on 1993-08-31. The listed applicant is Medical Sterile Products, Inc.. The 510(k) number is K931449.

When did MSP OPHTHALMIC (EYE SPUD) receive FDA 510(k) clearance?

MSP OPHTHALMIC (EYE SPUD) received FDA 510(k) clearance on 1993-08-31, under 510(k) number K931449.

Who is the listed applicant for MSP OPHTHALMIC (EYE SPUD)?

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

What is the FDA product code for MSP OPHTHALMIC (EYE SPUD)?

The FDA product code for MSP OPHTHALMIC (EYE SPUD) is HNA.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medical Sterile Products, 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.

K993122MSP M/K BLADE

Related Devices (Code: HNA)

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.

K874963MANUAL OPHTHALMIC SURGICAL INSTRUMENTSSolway, Inc.

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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