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FDA 510(k)

SABA INTIMA

K-Number: K924176 · 1993-12-23

Decision Date1993-12-23
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SABA INTIMA is the device name listed in this FDA 510(k) record. The listed applicant is Scott Paper Co.. It received FDA 510(k) clearance on 1993-12-23 under 510(k) number K924176. The device is classified under product code HHD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SABA INTIMA?

SABA INTIMA is a medical device that received FDA 510(k) clearance on 1993-12-23. The listed applicant is Scott Paper Co.. The 510(k) number is K924176.

When did SABA INTIMA receive FDA 510(k) clearance?

SABA INTIMA received FDA 510(k) clearance on 1993-12-23, under 510(k) number K924176.

Who is the listed applicant for SABA INTIMA?

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

What is the FDA product code for SABA INTIMA?

The FDA product code for SABA INTIMA is HHD.

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 Scott Paper 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.

Related Devices (Code: HHD)

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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