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FDA 510(k)

PEDIATRIC DIAG. CRITERIA OPTION 5600C

K-Number: K841416 · 1984-10-18

ApplicantHewlett-Packard Co.
Decision Date1984-10-18
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC DIAG. CRITERIA OPTION 5600C 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 1984-10-18 under 510(k) number K841416. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC DIAG. CRITERIA OPTION 5600C?

PEDIATRIC DIAG. CRITERIA OPTION 5600C is a medical device that received FDA 510(k) clearance on 1984-10-18. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K841416.

When did PEDIATRIC DIAG. CRITERIA OPTION 5600C receive FDA 510(k) clearance?

PEDIATRIC DIAG. CRITERIA OPTION 5600C received FDA 510(k) clearance on 1984-10-18, under 510(k) number K841416.

Who is the listed applicant for PEDIATRIC DIAG. CRITERIA OPTION 5600C?

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 PEDIATRIC DIAG. CRITERIA OPTION 5600C?

The FDA product code for PEDIATRIC DIAG. CRITERIA OPTION 5600C is DSI.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: DSI)

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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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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