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FDA 510(k)

BLACK OVAL-TOP TORP/PORP

K-Number: K934107 · 1994-06-08

Decision Date1994-06-08
Product CodeETA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BLACK OVAL-TOP TORP/PORP is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Richards, Inc.. It received FDA 510(k) clearance on 1994-06-08 under 510(k) number K934107. The device is classified under product code ETA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLACK OVAL-TOP TORP/PORP?

BLACK OVAL-TOP TORP/PORP is a medical device that received FDA 510(k) clearance on 1994-06-08. The listed applicant is Smith & Nephew Richards, Inc.. The 510(k) number is K934107.

When did BLACK OVAL-TOP TORP/PORP receive FDA 510(k) clearance?

BLACK OVAL-TOP TORP/PORP received FDA 510(k) clearance on 1994-06-08, under 510(k) number K934107.

Who is the listed applicant for BLACK OVAL-TOP TORP/PORP?

The FDA 510(k) record lists Smith & Nephew Richards, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLACK OVAL-TOP TORP/PORP?

The FDA product code for BLACK OVAL-TOP TORP/PORP is ETA.

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 Smith & Nephew Richards, 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.

View all 87 devices →

Related Devices (Code: ETA)

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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