UMBILICAL CORD CLAMP
K-Number: K781548 · 1978-10-17
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Device Summary
Frequently Asked Questions
What is the UMBILICAL CORD CLAMP?
UMBILICAL CORD CLAMP is a medical device that received FDA 510(k) clearance on 1978-10-17. The listed applicant is Hollister, Inc.. The 510(k) number is K781548.
When did UMBILICAL CORD CLAMP receive FDA 510(k) clearance?
UMBILICAL CORD CLAMP received FDA 510(k) clearance on 1978-10-17, under 510(k) number K781548.
Who is the listed applicant for UMBILICAL CORD CLAMP?
The FDA 510(k) record lists Hollister, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UMBILICAL CORD CLAMP?
The FDA product code for UMBILICAL CORD CLAMP 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 Hollister, Inc. 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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