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FDA 510(k)

SIMPLA TRIDENT LEG BAG + SIMPLA S6 BAG

K-Number: K925067 · 1993-06-10

Decision Date1993-06-10
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SIMPLA TRIDENT LEG BAG + SIMPLA S6 BAG is the device name listed in this FDA 510(k) record. The listed applicant is Simport Plastics, Ltd.. It received FDA 510(k) clearance on 1993-06-10 under 510(k) number K925067. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMPLA TRIDENT LEG BAG + SIMPLA S6 BAG?

SIMPLA TRIDENT LEG BAG + SIMPLA S6 BAG is a medical device that received FDA 510(k) clearance on 1993-06-10. The listed applicant is Simport Plastics, Ltd.. The 510(k) number is K925067.

When did SIMPLA TRIDENT LEG BAG + SIMPLA S6 BAG receive FDA 510(k) clearance?

SIMPLA TRIDENT LEG BAG + SIMPLA S6 BAG received FDA 510(k) clearance on 1993-06-10, under 510(k) number K925067.

Who is the listed applicant for SIMPLA TRIDENT LEG BAG + SIMPLA S6 BAG?

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

What is the FDA product code for SIMPLA TRIDENT LEG BAG + SIMPLA S6 BAG?

The FDA product code for SIMPLA TRIDENT LEG BAG + SIMPLA S6 BAG is KNX.

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.

Related Devices (Code: KNX)

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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