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FDA 510(k)

AUTOMOBILE LIGHTER POWER CORD

K-Number: K060549 · 2006-05-04

ApplicantPulmonetic Systems, Inc.
Decision Date2006-05-04
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTOMOBILE LIGHTER POWER CORD is the device name listed in this FDA 510(k) record. The listed applicant is Pulmonetic Systems, Inc.. It received FDA 510(k) clearance on 2006-05-04 under 510(k) number K060549. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMOBILE LIGHTER POWER CORD?

AUTOMOBILE LIGHTER POWER CORD is a medical device that received FDA 510(k) clearance on 2006-05-04. The listed applicant is Pulmonetic Systems, Inc.. The 510(k) number is K060549.

When did AUTOMOBILE LIGHTER POWER CORD receive FDA 510(k) clearance?

AUTOMOBILE LIGHTER POWER CORD received FDA 510(k) clearance on 2006-05-04, under 510(k) number K060549.

Who is the listed applicant for AUTOMOBILE LIGHTER POWER CORD?

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

What is the FDA product code for AUTOMOBILE LIGHTER POWER CORD?

The FDA product code for AUTOMOBILE LIGHTER POWER CORD is CBK.

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Other records listing Pulmonetic Systems, Inc. as applicant

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Related Devices (Code: CBK)

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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