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FDA 510(k)

SIEMENS SEVOFLURANE VAPORIZER SV 953

K-Number: K980884 · 1998-08-19

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1998-08-19
Product CodeCAD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIEMENS SEVOFLURANE VAPORIZER SV 953 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1998-08-19 under 510(k) number K980884. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS SEVOFLURANE VAPORIZER SV 953?

SIEMENS SEVOFLURANE VAPORIZER SV 953 is a medical device that received FDA 510(k) clearance on 1998-08-19. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K980884.

When did SIEMENS SEVOFLURANE VAPORIZER SV 953 receive FDA 510(k) clearance?

SIEMENS SEVOFLURANE VAPORIZER SV 953 received FDA 510(k) clearance on 1998-08-19, under 510(k) number K980884.

Who is the listed applicant for SIEMENS SEVOFLURANE VAPORIZER SV 953?

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

What is the FDA product code for SIEMENS SEVOFLURANE VAPORIZER SV 953?

The FDA product code for SIEMENS SEVOFLURANE VAPORIZER SV 953 is CAD.

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Related Devices (Code: CAD)

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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