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FDA 510(k)

MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE

K-Number: K954940 · 1996-01-17

Decision Date1996-01-17
Product CodeFTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is Mdt Biologic Co.. It received FDA 510(k) clearance on 1996-01-17 under 510(k) number K954940. The device is classified under product code FTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE?

MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE is a medical device that received FDA 510(k) clearance on 1996-01-17. The listed applicant is Mdt Biologic Co.. The 510(k) number is K954940.

When did MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE receive FDA 510(k) clearance?

MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE received FDA 510(k) clearance on 1996-01-17, under 510(k) number K954940.

Who is the listed applicant for MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE?

The FDA 510(k) record lists Mdt Biologic Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE?

The FDA product code for MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLE is FTA.

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 Mdt Biologic Co. 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 8 devices →

Related Devices (Code: FTA)

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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