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FDA 510(k)

MSI STERILE BACK SURGICAL GOWN PACK HAND TOWEL

K-Number: K912803 · 1992-01-10

Decision Date1992-01-10
Product CodeFYA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MSI STERILE BACK SURGICAL GOWN PACK HAND TOWEL is the device name listed in this FDA 510(k) record. The listed applicant is Medical Sterilization, Inc.. It received FDA 510(k) clearance on 1992-01-10 under 510(k) number K912803. The device is classified under product code FYA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MSI STERILE BACK SURGICAL GOWN PACK HAND TOWEL?

MSI STERILE BACK SURGICAL GOWN PACK HAND TOWEL is a medical device that received FDA 510(k) clearance on 1992-01-10. The listed applicant is Medical Sterilization, Inc.. The 510(k) number is K912803.

When did MSI STERILE BACK SURGICAL GOWN PACK HAND TOWEL receive FDA 510(k) clearance?

MSI STERILE BACK SURGICAL GOWN PACK HAND TOWEL received FDA 510(k) clearance on 1992-01-10, under 510(k) number K912803.

Who is the listed applicant for MSI STERILE BACK SURGICAL GOWN PACK HAND TOWEL?

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

What is the FDA product code for MSI STERILE BACK SURGICAL GOWN PACK HAND TOWEL?

The FDA product code for MSI STERILE BACK SURGICAL GOWN PACK HAND TOWEL is FYA.

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.

Other records listing Medical Sterilization, 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.

Related Devices (Code: FYA)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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