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FDA 510(k)

SIGNAL DISTRIBUTION NETWORK #78581A

K-Number: K822695 · 1982-10-15

Decision Date1982-10-15
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIGNAL DISTRIBUTION NETWORK #78581A 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 1982-10-15 under 510(k) number K822695. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGNAL DISTRIBUTION NETWORK #78581A?

SIGNAL DISTRIBUTION NETWORK #78581A is a medical device that received FDA 510(k) clearance on 1982-10-15. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K822695.

When did SIGNAL DISTRIBUTION NETWORK #78581A receive FDA 510(k) clearance?

SIGNAL DISTRIBUTION NETWORK #78581A received FDA 510(k) clearance on 1982-10-15, under 510(k) number K822695.

Who is the listed applicant for SIGNAL DISTRIBUTION NETWORK #78581A?

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 SIGNAL DISTRIBUTION NETWORK #78581A?

The FDA product code for SIGNAL DISTRIBUTION NETWORK #78581A is DRT.

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 Hewlett-Packard Co. 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 230 devices →

Related Devices (Code: DRT)

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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