SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540
K-Number: K994263 · 2000-01-24
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Device Summary
Frequently Asked Questions
What is the SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540?
SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540 is a medical device that received FDA 510(k) clearance on 2000-01-24. The listed applicant is Precision Dynamics Corp.. The 510(k) number is K994263.
When did SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540 receive FDA 510(k) clearance?
SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540 received FDA 510(k) clearance on 2000-01-24, under 510(k) number K994263.
Who is the listed applicant for SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540?
The FDA 510(k) record lists Precision Dynamics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540?
The FDA product code for SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540 is HFW.
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 Precision Dynamics 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: HFW)
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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