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FDA 510(k)

PDM-1 DEVICE:CAPD DISINFECTING DEVICE, MODIFIED

K-Number: K913110 · 1991-10-10

ApplicantMicrowave Medical Systems, Inc.
Decision Date1991-10-10
Product CodeDRQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PDM-1 DEVICE:CAPD DISINFECTING DEVICE, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Microwave Medical Systems, Inc.. It received FDA 510(k) clearance on 1991-10-10 under 510(k) number K913110. 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 PDM-1 DEVICE:CAPD DISINFECTING DEVICE, MODIFIED?

PDM-1 DEVICE:CAPD DISINFECTING DEVICE, MODIFIED is a medical device that received FDA 510(k) clearance on 1991-10-10. The listed applicant is Microwave Medical Systems, Inc.. The 510(k) number is K913110.

When did PDM-1 DEVICE:CAPD DISINFECTING DEVICE, MODIFIED receive FDA 510(k) clearance?

PDM-1 DEVICE:CAPD DISINFECTING DEVICE, MODIFIED received FDA 510(k) clearance on 1991-10-10, under 510(k) number K913110.

Who is the listed applicant for PDM-1 DEVICE:CAPD DISINFECTING DEVICE, MODIFIED?

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

What is the FDA product code for PDM-1 DEVICE:CAPD DISINFECTING DEVICE, MODIFIED?

The FDA product code for PDM-1 DEVICE:CAPD DISINFECTING DEVICE, MODIFIED is DRQ.

Related Clinical Trials

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Other records listing Microwave Medical Systems, 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.

K974387PDM3 DISINFECTION SYSTEM FOR PERITONEAL DIALYSIS EXCHANGES, PATIENT TRANSFER SET PTS102, CAP, HIGH TEMPERATUREK932083XDCS-100K914867QWIK-1(TM) IN-LINE IV FLUID WARMERK900295PERITONEAL DIALYSIS STYSTEM AND ACCESSORIES

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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