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FDA 510(k)

MODEL IPM-1 IMPEDANCE PULSE MONITOR

K-Number: K932438 · 1993-12-03

Decision Date1993-12-03
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL IPM-1 IMPEDANCE PULSE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Diagnostic Instruments. It received FDA 510(k) clearance on 1993-12-03 under 510(k) number K932438. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL IPM-1 IMPEDANCE PULSE MONITOR?

MODEL IPM-1 IMPEDANCE PULSE MONITOR is a medical device that received FDA 510(k) clearance on 1993-12-03. The listed applicant is Electro-Diagnostic Instruments. The 510(k) number is K932438.

When did MODEL IPM-1 IMPEDANCE PULSE MONITOR receive FDA 510(k) clearance?

MODEL IPM-1 IMPEDANCE PULSE MONITOR received FDA 510(k) clearance on 1993-12-03, under 510(k) number K932438.

Who is the listed applicant for MODEL IPM-1 IMPEDANCE PULSE MONITOR?

The FDA 510(k) record lists Electro-Diagnostic Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL IPM-1 IMPEDANCE PULSE MONITOR?

The FDA product code for MODEL IPM-1 IMPEDANCE PULSE MONITOR is DSB.

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.

Other records listing Electro-Diagnostic Instruments 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.

Related Devices (Code: DSB)

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.

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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