FDA 510(k)

MODIFIED USE OF TRIANGLE BANDAGE STERILE

K-Number: K874161 · 1987-12-04

Decision Date1987-12-04

Product CodeNAD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MODIFIED USE OF TRIANGLE BANDAGE STERILE is the device name listed in this FDA 510(k) record. The listed applicant is K. W. Griffen Co.. It received FDA 510(k) clearance on 1987-12-04 under 510(k) number K874161. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED USE OF TRIANGLE BANDAGE STERILE?

MODIFIED USE OF TRIANGLE BANDAGE STERILE is a medical device that received FDA 510(k) clearance on 1987-12-04. The listed applicant is K. W. Griffen Co.. The 510(k) number is K874161.

When did MODIFIED USE OF TRIANGLE BANDAGE STERILE receive FDA 510(k) clearance?

MODIFIED USE OF TRIANGLE BANDAGE STERILE received FDA 510(k) clearance on 1987-12-04, under 510(k) number K874161.

Who is the listed applicant for MODIFIED USE OF TRIANGLE BANDAGE STERILE?

The FDA 510(k) record lists K. W. Griffen Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED USE OF TRIANGLE BANDAGE STERILE?

The FDA product code for MODIFIED USE OF TRIANGLE BANDAGE STERILE is NAD.

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Related Devices (Code: NAD)

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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.