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FDA 510(k)

TUBE-BANDAGE FOR HUMAN DIGITS 200

K-Number: K840107 · 1984-04-25

ApplicantZens Health Care Products
Decision Date1984-04-25
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TUBE-BANDAGE FOR HUMAN DIGITS 200 is the device name listed in this FDA 510(k) record. The listed applicant is Zens Health Care Products. It received FDA 510(k) clearance on 1984-04-25 under 510(k) number K840107. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBE-BANDAGE FOR HUMAN DIGITS 200?

TUBE-BANDAGE FOR HUMAN DIGITS 200 is a medical device that received FDA 510(k) clearance on 1984-04-25. The listed applicant is Zens Health Care Products. The 510(k) number is K840107.

When did TUBE-BANDAGE FOR HUMAN DIGITS 200 receive FDA 510(k) clearance?

TUBE-BANDAGE FOR HUMAN DIGITS 200 received FDA 510(k) clearance on 1984-04-25, under 510(k) number K840107.

Who is the listed applicant for TUBE-BANDAGE FOR HUMAN DIGITS 200?

The FDA 510(k) record lists Zens Health Care Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TUBE-BANDAGE FOR HUMAN DIGITS 200?

The FDA product code for TUBE-BANDAGE FOR HUMAN DIGITS 200 is FQM.

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Related Devices (Code: FQM)

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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.

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