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FDA 510(k)

SAXON ULTRA THIN

K-Number: K900360 · 1990-04-02

ApplicantSafetex Corp.
Decision Date1990-04-02
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SAXON ULTRA THIN is the device name listed in this FDA 510(k) record. The listed applicant is Safetex Corp.. It received FDA 510(k) clearance on 1990-04-02 under 510(k) number K900360. The device is classified under product code HIS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAXON ULTRA THIN?

SAXON ULTRA THIN is a medical device that received FDA 510(k) clearance on 1990-04-02. The listed applicant is Safetex Corp.. The 510(k) number is K900360.

When did SAXON ULTRA THIN receive FDA 510(k) clearance?

SAXON ULTRA THIN received FDA 510(k) clearance on 1990-04-02, under 510(k) number K900360.

Who is the listed applicant for SAXON ULTRA THIN?

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

What is the FDA product code for SAXON ULTRA THIN?

The FDA product code for SAXON ULTRA THIN is HIS.

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 Safetex 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.

View all 7 devices →

Related Devices (Code: HIS)

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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