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FDA 510(k)

ID BRACLETS, ADULT & INFANT

K-Number: K771158 · 1977-10-13

ApplicantDivers-A-Med
Decision Date1977-10-13
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ID BRACLETS, ADULT & INFANT is the device name listed in this FDA 510(k) record. The listed applicant is Divers-A-Med. It received FDA 510(k) clearance on 1977-10-13 under 510(k) number K771158. The device is classified under product code LDR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ID BRACLETS, ADULT & INFANT?

ID BRACLETS, ADULT & INFANT is a medical device that received FDA 510(k) clearance on 1977-10-13. The listed applicant is Divers-A-Med. The 510(k) number is K771158.

When did ID BRACLETS, ADULT & INFANT receive FDA 510(k) clearance?

ID BRACLETS, ADULT & INFANT received FDA 510(k) clearance on 1977-10-13, under 510(k) number K771158.

Who is the listed applicant for ID BRACLETS, ADULT & INFANT?

The FDA 510(k) record lists Divers-A-Med as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ID BRACLETS, ADULT & INFANT?

The FDA product code for ID BRACLETS, ADULT & INFANT is LDR.

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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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