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FDA 510(k)

BEDDING PADS EGGCREATE PADS

K-Number: K802781 · 1980-12-10

ApplicantLeemart Bedding Mfg. Co.
Decision Date1980-12-10
Product CodeIKY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BEDDING PADS EGGCREATE PADS is the device name listed in this FDA 510(k) record. The listed applicant is Leemart Bedding Mfg. Co.. It received FDA 510(k) clearance on 1980-12-10 under 510(k) number K802781. The device is classified under product code IKY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEDDING PADS EGGCREATE PADS?

BEDDING PADS EGGCREATE PADS is a medical device that received FDA 510(k) clearance on 1980-12-10. The listed applicant is Leemart Bedding Mfg. Co.. The 510(k) number is K802781.

When did BEDDING PADS EGGCREATE PADS receive FDA 510(k) clearance?

BEDDING PADS EGGCREATE PADS received FDA 510(k) clearance on 1980-12-10, under 510(k) number K802781.

Who is the listed applicant for BEDDING PADS EGGCREATE PADS?

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

What is the FDA product code for BEDDING PADS EGGCREATE PADS?

The FDA product code for BEDDING PADS EGGCREATE PADS is IKY.

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Related Devices (Code: IKY)

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.

K914921SCM-3 AND ACCESSORIESGaymar Industries, Inc.K813226GEL FLOTATION MATTRESSJefferson Industries, Inc.K802833TETRA NATAL-MAT WATER FLOTATION MAT.Tetra Group U.S.A., Inc.K780779ECONO-FLOAT WATER FLOTATION MATTRESSJefferson Industries, Inc.K772062NEONATAL FLOTATION SYSTEMMedpro, Inc.K771824MEDPRO FLOTATION SYSTEMMedpro, Inc.

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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