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FDA 510(k)

ODIS - OBSTETRICAL DISPLAY INFO SYSTEM, HP M1370A

K-Number: K892354 · 1989-08-08

ApplicantHewlett-Packard Co.
Decision Date1989-08-08
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ODIS - OBSTETRICAL DISPLAY INFO SYSTEM, HP M1370A is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1989-08-08 under 510(k) number K892354. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ODIS - OBSTETRICAL DISPLAY INFO SYSTEM, HP M1370A?

ODIS - OBSTETRICAL DISPLAY INFO SYSTEM, HP M1370A is a medical device that received FDA 510(k) clearance on 1989-08-08. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K892354.

When did ODIS - OBSTETRICAL DISPLAY INFO SYSTEM, HP M1370A receive FDA 510(k) clearance?

ODIS - OBSTETRICAL DISPLAY INFO SYSTEM, HP M1370A received FDA 510(k) clearance on 1989-08-08, under 510(k) number K892354.

Who is the listed applicant for ODIS - OBSTETRICAL DISPLAY INFO SYSTEM, HP M1370A?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ODIS - OBSTETRICAL DISPLAY INFO SYSTEM, HP M1370A?

The FDA product code for ODIS - OBSTETRICAL DISPLAY INFO SYSTEM, HP M1370A is HGM.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: HGM)

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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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