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FDA 510(k)

SILENT PARTNER MODEL 10-2001

K-Number: K861011 · 1986-04-04

Decision Date1986-04-04
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SILENT PARTNER MODEL 10-2001 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1986-04-04 under 510(k) number K861011. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILENT PARTNER MODEL 10-2001?

SILENT PARTNER MODEL 10-2001 is a medical device that received FDA 510(k) clearance on 1986-04-04. The listed applicant is Medical Devices, Inc.. The 510(k) number is K861011.

When did SILENT PARTNER MODEL 10-2001 receive FDA 510(k) clearance?

SILENT PARTNER MODEL 10-2001 received FDA 510(k) clearance on 1986-04-04, under 510(k) number K861011.

Who is the listed applicant for SILENT PARTNER MODEL 10-2001?

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

What is the FDA product code for SILENT PARTNER MODEL 10-2001?

The FDA product code for SILENT PARTNER MODEL 10-2001 is CAW.

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 Medical Devices, Inc. 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 49 devices →

Related Devices (Code: CAW)

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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