'ECURLINE UMBILICAL CORD CLAMP #3500
K-Number: K990737 · 1999-04-06
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Device Summary
Frequently Asked Questions
What is the 'ECURLINE UMBILICAL CORD CLAMP #3500?
'ECURLINE UMBILICAL CORD CLAMP #3500 is a medical device that received FDA 510(k) clearance on 1999-04-06. The listed applicant is Precision Dynamics Corp.. The 510(k) number is K990737.
When did 'ECURLINE UMBILICAL CORD CLAMP #3500 receive FDA 510(k) clearance?
'ECURLINE UMBILICAL CORD CLAMP #3500 received FDA 510(k) clearance on 1999-04-06, under 510(k) number K990737.
Who is the listed applicant for 'ECURLINE UMBILICAL CORD CLAMP #3500?
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 'ECURLINE UMBILICAL CORD CLAMP #3500?
The FDA product code for 'ECURLINE UMBILICAL CORD CLAMP #3500 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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