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FDA 510(k)

PORTA GAS COMPRESSED GAS CYLINDER CART

K-Number: K910071 · 1991-03-22

Decision Date1991-03-22
Product CodeGET
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PORTA GAS COMPRESSED GAS CYLINDER CART is the device name listed in this FDA 510(k) record. The listed applicant is Sen Tech Medical Corp.. It received FDA 510(k) clearance on 1991-03-22 under 510(k) number K910071. The device is classified under product code GET. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTA GAS COMPRESSED GAS CYLINDER CART?

PORTA GAS COMPRESSED GAS CYLINDER CART is a medical device that received FDA 510(k) clearance on 1991-03-22. The listed applicant is Sen Tech Medical Corp.. The 510(k) number is K910071.

When did PORTA GAS COMPRESSED GAS CYLINDER CART receive FDA 510(k) clearance?

PORTA GAS COMPRESSED GAS CYLINDER CART received FDA 510(k) clearance on 1991-03-22, under 510(k) number K910071.

Who is the listed applicant for PORTA GAS COMPRESSED GAS CYLINDER CART?

The FDA 510(k) record lists Sen Tech Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTA GAS COMPRESSED GAS CYLINDER CART?

The FDA product code for PORTA GAS COMPRESSED GAS CYLINDER CART is GET.

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 Sen Tech Medical Corp. 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.

Related Devices (Code: GET)

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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