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FDA 510(k)

INSUFFLATOR FILTER TUBING SET

K-Number: K945970 · 1994-12-15

ApplicantXylog Corp.
Decision Date1994-12-15
Product CodeFCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INSUFFLATOR FILTER TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Xylog Corp.. It received FDA 510(k) clearance on 1994-12-15 under 510(k) number K945970. The device is classified under product code FCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSUFFLATOR FILTER TUBING SET?

INSUFFLATOR FILTER TUBING SET is a medical device that received FDA 510(k) clearance on 1994-12-15. The listed applicant is Xylog Corp.. The 510(k) number is K945970.

When did INSUFFLATOR FILTER TUBING SET receive FDA 510(k) clearance?

INSUFFLATOR FILTER TUBING SET received FDA 510(k) clearance on 1994-12-15, under 510(k) number K945970.

Who is the listed applicant for INSUFFLATOR FILTER TUBING SET?

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

What is the FDA product code for INSUFFLATOR FILTER TUBING SET?

The FDA product code for INSUFFLATOR FILTER TUBING SET is FCX.

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 Xylog 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: FCX)

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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