TUBING PACK, EXTRACORPOREAL, H-3000
K-Number: K770720 · 1977-08-04
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Device Summary
Frequently Asked Questions
What is the TUBING PACK, EXTRACORPOREAL, H-3000?
TUBING PACK, EXTRACORPOREAL, H-3000 is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is William Harvey Life Products Corp.. The 510(k) number is K770720.
When did TUBING PACK, EXTRACORPOREAL, H-3000 receive FDA 510(k) clearance?
TUBING PACK, EXTRACORPOREAL, H-3000 received FDA 510(k) clearance on 1977-08-04, under 510(k) number K770720.
Who is the listed applicant for TUBING PACK, EXTRACORPOREAL, H-3000?
The FDA 510(k) record lists William Harvey Life Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TUBING PACK, EXTRACORPOREAL, H-3000?
The FDA product code for TUBING PACK, EXTRACORPOREAL, H-3000 is BYS.
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 William Harvey Life Products 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: BYS)
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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