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FDA 510(k)

MSP M/K BLADE

K-Number: K993122 · 2000-03-16

ApplicantMedical Sterile Products, Inc.
Decision Date2000-03-16
Product CodeHNO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MSP M/K BLADE 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 2000-03-16 under 510(k) number K993122. The device is classified under product code HNO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSP M/K BLADE?

MSP M/K BLADE is a medical device that received FDA 510(k) clearance on 2000-03-16. The listed applicant is Medical Sterile Products, Inc.. The 510(k) number is K993122.

When did MSP M/K BLADE receive FDA 510(k) clearance?

MSP M/K BLADE received FDA 510(k) clearance on 2000-03-16, under 510(k) number K993122.

Who is the listed applicant for MSP M/K BLADE?

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 M/K BLADE?

The FDA product code for MSP M/K BLADE is HNO.

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.

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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.

K931449MSP OPHTHALMIC (EYE SPUD)

Related Devices (Code: HNO)

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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