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FDA 510(k)

LAERDAL ALTERNATIVE POWER, 5-6 A,5-6 B,2000

K-Number: K930549 · 1993-06-18

ApplicantRustronics, Inc.
Decision Date1993-06-18
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LAERDAL ALTERNATIVE POWER, 5-6 A,5-6 B,2000 is the device name listed in this FDA 510(k) record. The listed applicant is Rustronics, Inc.. It received FDA 510(k) clearance on 1993-06-18 under 510(k) number K930549. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAERDAL ALTERNATIVE POWER, 5-6 A,5-6 B,2000?

LAERDAL ALTERNATIVE POWER, 5-6 A,5-6 B,2000 is a medical device that received FDA 510(k) clearance on 1993-06-18. The listed applicant is Rustronics, Inc.. The 510(k) number is K930549.

When did LAERDAL ALTERNATIVE POWER, 5-6 A,5-6 B,2000 receive FDA 510(k) clearance?

LAERDAL ALTERNATIVE POWER, 5-6 A,5-6 B,2000 received FDA 510(k) clearance on 1993-06-18, under 510(k) number K930549.

Who is the listed applicant for LAERDAL ALTERNATIVE POWER, 5-6 A,5-6 B,2000?

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

What is the FDA product code for LAERDAL ALTERNATIVE POWER, 5-6 A,5-6 B,2000?

The FDA product code for LAERDAL ALTERNATIVE POWER, 5-6 A,5-6 B,2000 is BTA.

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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.

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