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FDA 510(k)

HITACHI TECH-MOBLE DHC-121

K-Number: K780313 · 1978-03-14

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1978-03-14
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HITACHI TECH-MOBLE DHC-121 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1978-03-14 under 510(k) number K780313. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HITACHI TECH-MOBLE DHC-121?

HITACHI TECH-MOBLE DHC-121 is a medical device that received FDA 510(k) clearance on 1978-03-14. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K780313.

When did HITACHI TECH-MOBLE DHC-121 receive FDA 510(k) clearance?

HITACHI TECH-MOBLE DHC-121 received FDA 510(k) clearance on 1978-03-14, under 510(k) number K780313.

Who is the listed applicant for HITACHI TECH-MOBLE DHC-121?

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

What is the FDA product code for HITACHI TECH-MOBLE DHC-121?

The FDA product code for HITACHI TECH-MOBLE DHC-121 is IZL.

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Related Devices (Code: IZL)

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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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