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FDA 510(k)

BROWSER (EVENT SOFTWARE) MODEL # 4500E

K-Number: K982550 · 1998-10-05

ApplicantRespironics, Inc.
Decision Date1998-10-05
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

BROWSER (EVENT SOFTWARE) MODEL # 4500E is the device name listed in this FDA 510(k) record. The listed applicant is Respironics, Inc.. It received FDA 510(k) clearance on 1998-10-05 under 510(k) number K982550. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the BROWSER (EVENT SOFTWARE) MODEL # 4500E?

BROWSER (EVENT SOFTWARE) MODEL # 4500E is a medical device that received FDA 510(k) clearance on 1998-10-05. The listed applicant is Respironics, Inc.. The 510(k) number is K982550.

When did BROWSER (EVENT SOFTWARE) MODEL # 4500E receive FDA 510(k) clearance?

BROWSER (EVENT SOFTWARE) MODEL # 4500E received FDA 510(k) clearance on 1998-10-05, under 510(k) number K982550.

Who is the listed applicant for BROWSER (EVENT SOFTWARE) MODEL # 4500E?

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

What is the FDA product code for BROWSER (EVENT SOFTWARE) MODEL # 4500E?

The FDA product code for BROWSER (EVENT SOFTWARE) MODEL # 4500E is BZQ.

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Related Devices (Code: BZQ)

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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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