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FDA 510(k)

BOOM ARM

K-Number: K851621 · 1985-05-10

ApplicantDraeger Medical, Inc.
Decision Date1985-05-10
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BOOM ARM is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical, Inc.. It received FDA 510(k) clearance on 1985-05-10 under 510(k) number K851621. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOOM ARM?

BOOM ARM is a medical device that received FDA 510(k) clearance on 1985-05-10. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K851621.

When did BOOM ARM receive FDA 510(k) clearance?

BOOM ARM received FDA 510(k) clearance on 1985-05-10, under 510(k) number K851621.

Who is the listed applicant for BOOM ARM?

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

What is the FDA product code for BOOM ARM?

The FDA product code for BOOM ARM is BSZ.

Other records listing Draeger 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.

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Related Devices (Code: BSZ)

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.

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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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