FDA 510(k)

PLASTIC TUBING ADAPTERS 5-IN-1-

K-Number: K800880 · 1980-05-14

Decision Date1980-05-14

Product CodeDTL

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PLASTIC TUBING ADAPTERS 5-IN-1- is the device name listed in this FDA 510(k) record. The listed applicant is Harvard Laboratories. It received FDA 510(k) clearance on 1980-05-14 under 510(k) number K800880. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLASTIC TUBING ADAPTERS 5-IN-1-?

PLASTIC TUBING ADAPTERS 5-IN-1- is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is Harvard Laboratories. The 510(k) number is K800880.

When did PLASTIC TUBING ADAPTERS 5-IN-1- receive FDA 510(k) clearance?

PLASTIC TUBING ADAPTERS 5-IN-1- received FDA 510(k) clearance on 1980-05-14, under 510(k) number K800880.

Who is the listed applicant for PLASTIC TUBING ADAPTERS 5-IN-1-?

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 PLASTIC TUBING ADAPTERS 5-IN-1-?

The FDA product code for PLASTIC TUBING ADAPTERS 5-IN-1- is DTL.

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Other records listing Harvard Laboratories as applicant

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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.