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FDA 510(k)

PILLOW W/STAPHCHEK TICKING

K-Number: K842335 · 1984-08-01

Decision Date1984-08-01
Product CodeKME
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PILLOW W/STAPHCHEK TICKING is the device name listed in this FDA 510(k) record. The listed applicant is Monterey Mills, Inc.. It received FDA 510(k) clearance on 1984-08-01 under 510(k) number K842335. The device is classified under product code KME. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLOW W/STAPHCHEK TICKING?

PILLOW W/STAPHCHEK TICKING is a medical device that received FDA 510(k) clearance on 1984-08-01. The listed applicant is Monterey Mills, Inc.. The 510(k) number is K842335.

When did PILLOW W/STAPHCHEK TICKING receive FDA 510(k) clearance?

PILLOW W/STAPHCHEK TICKING received FDA 510(k) clearance on 1984-08-01, under 510(k) number K842335.

Who is the listed applicant for PILLOW W/STAPHCHEK TICKING?

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

What is the FDA product code for PILLOW W/STAPHCHEK TICKING?

The FDA product code for PILLOW W/STAPHCHEK TICKING is KME.

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 Monterey Mills, 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.

Related Devices (Code: KME)

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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