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FDA 510(k)

LEG BAG EXTENSION TUBE

K-Number: K802606 · 1980-10-31

Decision Date1980-10-31
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LEG BAG EXTENSION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Associated Medical Products Co.. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K802606. 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 LEG BAG EXTENSION TUBE?

LEG BAG EXTENSION TUBE is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is Associated Medical Products Co.. The 510(k) number is K802606.

When did LEG BAG EXTENSION TUBE receive FDA 510(k) clearance?

LEG BAG EXTENSION TUBE received FDA 510(k) clearance on 1980-10-31, under 510(k) number K802606.

Who is the listed applicant for LEG BAG EXTENSION TUBE?

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

What is the FDA product code for LEG BAG EXTENSION TUBE?

The FDA product code for LEG BAG EXTENSION TUBE 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.

Other records listing Associated Medical Products 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 29 devices →

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

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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