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FDA 510(k)

COBBLER'S CHIP SPLINTS

K-Number: K810110 · 1981-01-26

ApplicantSecol Co.
Decision Date1981-01-26
Product CodeLGF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COBBLER'S CHIP SPLINTS is the device name listed in this FDA 510(k) record. The listed applicant is Secol Co.. It received FDA 510(k) clearance on 1981-01-26 under 510(k) number K810110. The device is classified under product code LGF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COBBLER'S CHIP SPLINTS?

COBBLER'S CHIP SPLINTS is a medical device that received FDA 510(k) clearance on 1981-01-26. The listed applicant is Secol Co.. The 510(k) number is K810110.

When did COBBLER'S CHIP SPLINTS receive FDA 510(k) clearance?

COBBLER'S CHIP SPLINTS received FDA 510(k) clearance on 1981-01-26, under 510(k) number K810110.

Who is the listed applicant for COBBLER'S CHIP SPLINTS?

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 COBBLER'S CHIP SPLINTS?

The FDA product code for COBBLER'S CHIP SPLINTS is LGF.

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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 SPLINTSK802794PRO-OPHTA STICKSK802793LOMATUELL OINTMENT DRESSINGK802787METALLINE DRESSINGS

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Related Devices (Code: LGF)

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.

K043526SILVERSEAL TUBULAR WOUND DRESSING WITH X-STATICNoble Fiber Technologies, Inc.K973417CLINITEX STOCKINETTEClinitex Medical Corp.K973420CLINITEX CAST PADDINGClinitex Medical Corp.K955320PROTEC COTTON PADDING BANDAGEDerivadas Degasa S.A. DE C.V.K932507QUICK-CAST IMMOBILIZERLandec Corp.K931672CARAPACE STERILE CAST PADDINGCarapace, 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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