UMBILICAL CORD CLAMP AND CUTTER
K-Number: K901557 · 1990-05-15
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Device Summary
Frequently Asked Questions
What is the UMBILICAL CORD CLAMP AND CUTTER?
UMBILICAL CORD CLAMP AND CUTTER is a medical device that received FDA 510(k) clearance on 1990-05-15. The listed applicant is Microtek-Heritage, Inc.. The 510(k) number is K901557.
When did UMBILICAL CORD CLAMP AND CUTTER receive FDA 510(k) clearance?
UMBILICAL CORD CLAMP AND CUTTER received FDA 510(k) clearance on 1990-05-15, under 510(k) number K901557.
Who is the listed applicant for UMBILICAL CORD CLAMP AND CUTTER?
The FDA 510(k) record lists Microtek-Heritage, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UMBILICAL CORD CLAMP AND CUTTER?
The FDA product code for UMBILICAL CORD CLAMP AND CUTTER 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.
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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