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FDA 510(k)

ORTHOPEDIC PADDING

K-Number: K802795 · 1980-12-10

ApplicantSecol Co.
Decision Date1980-12-10
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ORTHOPEDIC PADDING is the device name listed in this FDA 510(k) record. The listed applicant is Secol Co.. It received FDA 510(k) clearance on 1980-12-10 under 510(k) number K802795. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOPEDIC PADDING?

ORTHOPEDIC PADDING is a medical device that received FDA 510(k) clearance on 1980-12-10. The listed applicant is Secol Co.. The 510(k) number is K802795.

When did ORTHOPEDIC PADDING receive FDA 510(k) clearance?

ORTHOPEDIC PADDING received FDA 510(k) clearance on 1980-12-10, under 510(k) number K802795.

Who is the listed applicant for ORTHOPEDIC PADDING?

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

What is the FDA product code for ORTHOPEDIC PADDING?

The FDA product code for ORTHOPEDIC PADDING is KGX.

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Other records listing Secol 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.

K802790SOLVALINEK810111CELLONA PLASTER VARNISHK810109METAL SPLINTSK810110COBBLER'S CHIP SPLINTSK802794PRO-OPHTA STICKSK802793LOMATUELL OINTMENT DRESSING

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Related Devices (Code: KGX)

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.

K001240SERAGARD INJECTION PATCHPlatinum Services, Inc.K983368CARE BAND ANTIBACTERIAL BANDAGESAso Corp.K972914SYVEK PATCHMarine Polymer Technologies, Inc.K943314ADHESIVE BANDAGES WITH OTC DRUGJohnson & Johnson Consumer Products, Inc.K952606TARGETT PATCHCutting Edge Technologies, Inc.K954007PARALLELJohnson & Johnson Consumer Products, 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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