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FDA 510(k)

BAGRIGHT RESPOSABLE CHILD RESUSCITATOR

K-Number: K961331 · 1996-06-28

Decision Date1996-06-28
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BAGRIGHT RESPOSABLE CHILD RESUSCITATOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Marketing Concepts. It received FDA 510(k) clearance on 1996-06-28 under 510(k) number K961331. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAGRIGHT RESPOSABLE CHILD RESUSCITATOR?

BAGRIGHT RESPOSABLE CHILD RESUSCITATOR is a medical device that received FDA 510(k) clearance on 1996-06-28. The listed applicant is Medical Marketing Concepts. The 510(k) number is K961331.

When did BAGRIGHT RESPOSABLE CHILD RESUSCITATOR receive FDA 510(k) clearance?

BAGRIGHT RESPOSABLE CHILD RESUSCITATOR received FDA 510(k) clearance on 1996-06-28, under 510(k) number K961331.

Who is the listed applicant for BAGRIGHT RESPOSABLE CHILD RESUSCITATOR?

The FDA 510(k) record lists Medical Marketing Concepts as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAGRIGHT RESPOSABLE CHILD RESUSCITATOR?

The FDA product code for BAGRIGHT RESPOSABLE CHILD RESUSCITATOR is BTM.

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 Medical Marketing Concepts 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.

View all 13 devices →

Related Devices (Code: BTM)

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

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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