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FDA 510(k)

ANESTHESIA EXTENSION TUBES

K-Number: K800877 · 1980-06-17

Decision Date1980-06-17
Product CodeFPK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA EXTENSION TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Harvard Laboratories. It received FDA 510(k) clearance on 1980-06-17 under 510(k) number K800877. The device is classified under product code FPK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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