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FDA 510(k)

SUNBEAM HEALTH MONITOR MODEL NO. 7600

K-Number: K852795 · 1985-11-18

Decision Date1985-11-18
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SUNBEAM HEALTH MONITOR MODEL NO. 7600 is the device name listed in this FDA 510(k) record. The listed applicant is Aanson Scale Co.. It received FDA 510(k) clearance on 1985-11-18 under 510(k) number K852795. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUNBEAM HEALTH MONITOR MODEL NO. 7600?

SUNBEAM HEALTH MONITOR MODEL NO. 7600 is a medical device that received FDA 510(k) clearance on 1985-11-18. The listed applicant is Aanson Scale Co.. The 510(k) number is K852795.

When did SUNBEAM HEALTH MONITOR MODEL NO. 7600 receive FDA 510(k) clearance?

SUNBEAM HEALTH MONITOR MODEL NO. 7600 received FDA 510(k) clearance on 1985-11-18, under 510(k) number K852795.

Who is the listed applicant for SUNBEAM HEALTH MONITOR MODEL NO. 7600?

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

What is the FDA product code for SUNBEAM HEALTH MONITOR MODEL NO. 7600?

The FDA product code for SUNBEAM HEALTH MONITOR MODEL NO. 7600 is DXN.

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.

Related Devices (Code: DXN)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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