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FDA 510(k)

3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP

K-Number: K132967 · 2013-12-06

Decision Date2013-12-06
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP is the device name listed in this FDA 510(k) record. The listed applicant is 3B Medical, Inc.. It received FDA 510(k) clearance on 2013-12-06 under 510(k) number K132967. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP?

3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP is a medical device that received FDA 510(k) clearance on 2013-12-06. The listed applicant is 3B Medical, Inc.. The 510(k) number is K132967.

When did 3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP receive FDA 510(k) clearance?

3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP received FDA 510(k) clearance on 2013-12-06, under 510(k) number K132967.

Who is the listed applicant for 3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP?

The FDA 510(k) record lists 3B Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP?

The FDA product code for 3B RESMART CPAP AND AUTO CPAP, BMC RESMART CPAP AND AUTO CPAP is BZD.

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 3B Medical, Inc. 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 8 devices →

Related Devices (Code: BZD)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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