ANESTHESIA EXTENSION TUBES
K-Number: K800877 · 1980-06-17
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Device Summary
Frequently Asked Questions
What is the ANESTHESIA EXTENSION TUBES?
ANESTHESIA EXTENSION TUBES is a medical device that received FDA 510(k) clearance on 1980-06-17. The listed applicant is Harvard Laboratories. The 510(k) number is K800877.
When did ANESTHESIA EXTENSION TUBES receive FDA 510(k) clearance?
ANESTHESIA EXTENSION TUBES received FDA 510(k) clearance on 1980-06-17, under 510(k) number K800877.
Who is the listed applicant for ANESTHESIA EXTENSION TUBES?
The FDA 510(k) record lists Harvard Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANESTHESIA EXTENSION TUBES?
The FDA product code for ANESTHESIA EXTENSION TUBES is FPK.
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 Harvard Laboratories 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: FPK)
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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