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FDA 510(k)

PERITEMP PF 4005 HEATER

K-Number: K932068 · 1993-12-07

ApplicantPerimed, Inc.
Decision Date1993-12-07
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERITEMP PF 4005 HEATER is the device name listed in this FDA 510(k) record. The listed applicant is Perimed, Inc.. It received FDA 510(k) clearance on 1993-12-07 under 510(k) number K932068. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERITEMP PF 4005 HEATER?

PERITEMP PF 4005 HEATER is a medical device that received FDA 510(k) clearance on 1993-12-07. The listed applicant is Perimed, Inc.. The 510(k) number is K932068.

When did PERITEMP PF 4005 HEATER receive FDA 510(k) clearance?

PERITEMP PF 4005 HEATER received FDA 510(k) clearance on 1993-12-07, under 510(k) number K932068.

Who is the listed applicant for PERITEMP PF 4005 HEATER?

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

What is the FDA product code for PERITEMP PF 4005 HEATER?

The FDA product code for PERITEMP PF 4005 HEATER is DPW.

Related Clinical Trials

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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Other records listing Perimed, 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.

K990960PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)K974285PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNITK935495PF404/409/410/411/416/418 W/PF319:0/319:1/319:2K922368PERIFLUX PF4001 LASER DOPPLER FLOWMETERK890828PERIFLUX PF3

Related Devices (Code: DPW)

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.

K260700BlueDop Vascular ExpertBlueDop Medical, Ltd.K252810FloPatch FP120Flosonics MedicalK251904VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01)Remington Medical, Inc.K251114FloPatch FP120Flosonics MedicalK243852Elfor-LElfi-Tech , Ltd.K241583VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-CP-01, VC-CH-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-SP-01, VC-CH-01)Remington Medical, 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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