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FDA 510(k)

CATH BELT PD CATHETER AND TRANSFER SET HOLDER

K-Number: K930175 · 1994-06-23

Decision Date1994-06-23
Product CodeFJS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATH BELT PD CATHETER AND TRANSFER SET HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Tabex Industries, Inc.. It received FDA 510(k) clearance on 1994-06-23 under 510(k) number K930175. The device is classified under product code FJS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATH BELT PD CATHETER AND TRANSFER SET HOLDER?

CATH BELT PD CATHETER AND TRANSFER SET HOLDER is a medical device that received FDA 510(k) clearance on 1994-06-23. The listed applicant is Tabex Industries, Inc.. The 510(k) number is K930175.

When did CATH BELT PD CATHETER AND TRANSFER SET HOLDER receive FDA 510(k) clearance?

CATH BELT PD CATHETER AND TRANSFER SET HOLDER received FDA 510(k) clearance on 1994-06-23, under 510(k) number K930175.

Who is the listed applicant for CATH BELT PD CATHETER AND TRANSFER SET HOLDER?

The FDA 510(k) record lists Tabex Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATH BELT PD CATHETER AND TRANSFER SET HOLDER?

The FDA product code for CATH BELT PD CATHETER AND TRANSFER SET HOLDER is FJS.

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 Tabex Industries, 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.

Related Devices (Code: FJS)

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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