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FDA 510(k)

STERILE EQUIPMENT COVERS

K-Number: K931417 · 1995-07-06

Decision Date1995-07-06
Product CodeMMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE EQUIPMENT COVERS is the device name listed in this FDA 510(k) record. The listed applicant is Custom Medical Products, Ltd.. It received FDA 510(k) clearance on 1995-07-06 under 510(k) number K931417. The device is classified under product code MMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE EQUIPMENT COVERS?

STERILE EQUIPMENT COVERS is a medical device that received FDA 510(k) clearance on 1995-07-06. The listed applicant is Custom Medical Products, Ltd.. The 510(k) number is K931417.

When did STERILE EQUIPMENT COVERS receive FDA 510(k) clearance?

STERILE EQUIPMENT COVERS received FDA 510(k) clearance on 1995-07-06, under 510(k) number K931417.

Who is the listed applicant for STERILE EQUIPMENT COVERS?

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

What is the FDA product code for STERILE EQUIPMENT COVERS?

The FDA product code for STERILE EQUIPMENT COVERS is MMP.

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 Custom Medical Products, Ltd. 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.

View all 13 devices →

Related Devices (Code: MMP)

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

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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