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FDA 510(k)

SFA-II MICROPROCESSOR-CONTROLLED MODULE

K-Number: K910905 · 1991-07-24

ApplicantLife Sciences Manufacturing, Inc.
Decision Date1991-07-24
Product CodeDRQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SFA-II MICROPROCESSOR-CONTROLLED MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Life Sciences Manufacturing, Inc.. It received FDA 510(k) clearance on 1991-07-24 under 510(k) number K910905. The device is classified under product code DRQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SFA-II MICROPROCESSOR-CONTROLLED MODULE?

SFA-II MICROPROCESSOR-CONTROLLED MODULE is a medical device that received FDA 510(k) clearance on 1991-07-24. The listed applicant is Life Sciences Manufacturing, Inc.. The 510(k) number is K910905.

When did SFA-II MICROPROCESSOR-CONTROLLED MODULE receive FDA 510(k) clearance?

SFA-II MICROPROCESSOR-CONTROLLED MODULE received FDA 510(k) clearance on 1991-07-24, under 510(k) number K910905.

Who is the listed applicant for SFA-II MICROPROCESSOR-CONTROLLED MODULE?

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

What is the FDA product code for SFA-II MICROPROCESSOR-CONTROLLED MODULE?

The FDA product code for SFA-II MICROPROCESSOR-CONTROLLED MODULE is DRQ.

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Other records listing Life Sciences Manufacturing, Inc. as applicant

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.

K903700IPG-II MODULEK900365PAG MICROPROCESSOR-CONTROLLED MODULEK896500CWD/PPG MODULEK895588PORTABLE AIR PLETHYSMOGRAPHK896528SFA MODULEK884624MVL/MODULAB WITH PVR MODULE

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Related Devices (Code: DRQ)

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.

K172216ACIST RXi Mini SystemAcist Medical Systems, Inc.K050006BOREALIS AMPLIFIER (CLEARSIGN), MODEL 2001232 160 CHANNEL VERSION, 2001267 80 CHANNEL VERSION, 2001268 40 CHANNEL VERSIOC.R. Bard, Inc.K050974DRAEGER MEDICAL INFORMATION BUS (MIB, MIB II, MIB DUO) PROTOCOL CONVERTERSDraeger Medical Systems, Inc.K033807INFINITYEDICAL INFORMATION BUS (MIB/MIB II AND MIB DUO) PROTOCOL CONVERTERDraeger Medical Systems, Inc.K013205MILLAR PRESSURE CONTROL UNIT MODEL PCU-2000Millar Instruments, Inc.K020277SIEMENS MEDICAL INFROMATION BUS (MIB II) PROTOCOL CONVERTERSiemens Medical Solutions USA, Inc.

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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