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FDA 510(k)

TOA MEDICAL ELECTRONICS CA-5000

K-Number: K933886 · 1994-01-27

Decision Date1994-01-27
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TOA MEDICAL ELECTRONICS CA-5000 is the device name listed in this FDA 510(k) record. The listed applicant is Toa Medical Electronics USA, Inc.. It received FDA 510(k) clearance on 1994-01-27 under 510(k) number K933886. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOA MEDICAL ELECTRONICS CA-5000?

TOA MEDICAL ELECTRONICS CA-5000 is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Toa Medical Electronics USA, Inc.. The 510(k) number is K933886.

When did TOA MEDICAL ELECTRONICS CA-5000 receive FDA 510(k) clearance?

TOA MEDICAL ELECTRONICS CA-5000 received FDA 510(k) clearance on 1994-01-27, under 510(k) number K933886.

Who is the listed applicant for TOA MEDICAL ELECTRONICS CA-5000?

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

What is the FDA product code for TOA MEDICAL ELECTRONICS CA-5000?

The FDA product code for TOA MEDICAL ELECTRONICS CA-5000 is JPA.

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 Toa Medical Electronics USA, 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.

View all 33 devices →

Related Devices (Code: JPA)

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

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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