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FDA 510(k)

NORELCO CLEAN AIR SYSTEM

K-Number: K943238 · 1994-11-28

ApplicantPhilips Electronic North America Corp. (Pena)
Decision Date1994-11-28
Product CodeFRF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NORELCO CLEAN AIR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Philips Electronic North America Corp. (Pena). It received FDA 510(k) clearance on 1994-11-28 under 510(k) number K943238. The device is classified under product code FRF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORELCO CLEAN AIR SYSTEM?

NORELCO CLEAN AIR SYSTEM is a medical device that received FDA 510(k) clearance on 1994-11-28. The listed applicant is Philips Electronic North America Corp. (Pena). The 510(k) number is K943238.

When did NORELCO CLEAN AIR SYSTEM receive FDA 510(k) clearance?

NORELCO CLEAN AIR SYSTEM received FDA 510(k) clearance on 1994-11-28, under 510(k) number K943238.

Who is the listed applicant for NORELCO CLEAN AIR SYSTEM?

The FDA 510(k) record lists Philips Electronic North America Corp. (Pena) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NORELCO CLEAN AIR SYSTEM?

The FDA product code for NORELCO CLEAN AIR SYSTEM is FRF.

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Related Devices (Code: FRF)

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

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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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