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FDA 510(k)

REMSTAR WTIH RAMP AND REMOTE MODIFICATION

K-Number: K920699 · 1992-12-07

ApplicantRespironics, Inc.
Decision Date1992-12-07
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REMSTAR WTIH RAMP AND REMOTE MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Respironics, Inc.. It received FDA 510(k) clearance on 1992-12-07 under 510(k) number K920699. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REMSTAR WTIH RAMP AND REMOTE MODIFICATION?

REMSTAR WTIH RAMP AND REMOTE MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-12-07. The listed applicant is Respironics, Inc.. The 510(k) number is K920699.

When did REMSTAR WTIH RAMP AND REMOTE MODIFICATION receive FDA 510(k) clearance?

REMSTAR WTIH RAMP AND REMOTE MODIFICATION received FDA 510(k) clearance on 1992-12-07, under 510(k) number K920699.

Who is the listed applicant for REMSTAR WTIH RAMP AND REMOTE MODIFICATION?

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 REMSTAR WTIH RAMP AND REMOTE MODIFICATION?

The FDA product code for REMSTAR WTIH RAMP AND REMOTE MODIFICATION is BZD.

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Related Devices (Code: BZD)

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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