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FDA 510(k)

SCOOTER BOARD

K-Number: K811489 · 1981-06-12

ApplicantFred Sammons, Inc.
Decision Date1981-06-12
Product CodeKNL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SCOOTER BOARD is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1981-06-12 under 510(k) number K811489. The device is classified under product code KNL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCOOTER BOARD?

SCOOTER BOARD is a medical device that received FDA 510(k) clearance on 1981-06-12. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K811489.

When did SCOOTER BOARD receive FDA 510(k) clearance?

SCOOTER BOARD received FDA 510(k) clearance on 1981-06-12, under 510(k) number K811489.

Who is the listed applicant for SCOOTER BOARD?

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

What is the FDA product code for SCOOTER BOARD?

The FDA product code for SCOOTER BOARD is KNL.

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.

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Other records listing Fred Sammons, 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.

K880644ULTRA-PAN FOR ORTHOTIC PLASTICS (7262)K880647ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)K831549ARM SLINGSK831548SPLINTSK831550FINGER BONIOMETER BK7506K831544DELUXE TRACTION EXERCISE GLOVE BK5035

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Related Devices (Code: KNL)

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.

K841695CRAWLERMaddak, Inc.K790528THERAPY GYROSCOPEMaddak, Inc.K781198BOARD, SCOOTERFred Sammons, Inc.K780296THERAPY SCOOTERConvaid Product Development

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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