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FDA 510(k)

PHARMASEAL STERILE UMBILICAL CORD CLAMP

K-Number: K875166 · 1988-03-02

Decision Date1988-03-02
Product CodeHWI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PHARMASEAL STERILE UMBILICAL CORD CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1988-03-02 under 510(k) number K875166. The device is classified under product code HWI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHARMASEAL STERILE UMBILICAL CORD CLAMP?

PHARMASEAL STERILE UMBILICAL CORD CLAMP is a medical device that received FDA 510(k) clearance on 1988-03-02. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K875166.

When did PHARMASEAL STERILE UMBILICAL CORD CLAMP receive FDA 510(k) clearance?

PHARMASEAL STERILE UMBILICAL CORD CLAMP received FDA 510(k) clearance on 1988-03-02, under 510(k) number K875166.

Who is the listed applicant for PHARMASEAL STERILE UMBILICAL CORD CLAMP?

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

What is the FDA product code for PHARMASEAL STERILE UMBILICAL CORD CLAMP?

The FDA product code for PHARMASEAL STERILE UMBILICAL CORD CLAMP is HWI.

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 Baxter Healthcare 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.

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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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