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FDA 510(k)

SECONDARY I.V. TUBING SETS

K-Number: K800878 · 1980-06-17

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

Device Summary

SECONDARY I.V. TUBING SETS 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 K800878. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECONDARY I.V. TUBING SETS?

SECONDARY I.V. TUBING SETS 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 K800878.

When did SECONDARY I.V. TUBING SETS receive FDA 510(k) clearance?

SECONDARY I.V. TUBING SETS received FDA 510(k) clearance on 1980-06-17, under 510(k) number K800878.

Who is the listed applicant for SECONDARY I.V. TUBING SETS?

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 SECONDARY I.V. TUBING SETS?

The FDA product code for SECONDARY I.V. TUBING SETS is FPA.

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: FPA)

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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