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FDA 510(k)

MODEL 90421 FLEXPORT INTERFACE

K-Number: K903702 · 1990-10-19

ApplicantSpacelabs, Inc.
Decision Date1990-10-19
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 90421 FLEXPORT INTERFACE is the device name listed in this FDA 510(k) record. The listed applicant is Spacelabs, Inc.. It received FDA 510(k) clearance on 1990-10-19 under 510(k) number K903702. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 90421 FLEXPORT INTERFACE?

MODEL 90421 FLEXPORT INTERFACE is a medical device that received FDA 510(k) clearance on 1990-10-19. The listed applicant is Spacelabs, Inc.. The 510(k) number is K903702.

When did MODEL 90421 FLEXPORT INTERFACE receive FDA 510(k) clearance?

MODEL 90421 FLEXPORT INTERFACE received FDA 510(k) clearance on 1990-10-19, under 510(k) number K903702.

Who is the listed applicant for MODEL 90421 FLEXPORT INTERFACE?

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

What is the FDA product code for MODEL 90421 FLEXPORT INTERFACE?

The FDA product code for MODEL 90421 FLEXPORT INTERFACE is DQA.

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Other records listing Spacelabs, Inc. as applicant

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K954962SPACELABS MEDICAL MULTIGAS ANALYZERK951605SPACELABS MEDICAL CASEMASTER INFORMATION MANAGEMENT SYSTEMK950779HEART RATE VARIABILITY SOFTWARE OPTIONK941165COMET CAPNOGRAPH MODULEK923788SPACE LABS MODEL 90560K912742ESOPHAGEAL STETHOSCOPE TEMPERATURE PROBE

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Related Devices (Code: DQA)

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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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