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FDA 510(k)

DELUXE ADJUST-ANGLE BOARD-BK4066

K-Number: K831538 · 1983-06-08

ApplicantFred Sammons, Inc.
Decision Date1983-06-08
Product CodeION
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DELUXE ADJUST-ANGLE BOARD-BK4066 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 1983-06-08 under 510(k) number K831538. The device is classified under product code ION. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELUXE ADJUST-ANGLE BOARD-BK4066?

DELUXE ADJUST-ANGLE BOARD-BK4066 is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K831538.

When did DELUXE ADJUST-ANGLE BOARD-BK4066 receive FDA 510(k) clearance?

DELUXE ADJUST-ANGLE BOARD-BK4066 received FDA 510(k) clearance on 1983-06-08, under 510(k) number K831538.

Who is the listed applicant for DELUXE ADJUST-ANGLE BOARD-BK4066?

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 DELUXE ADJUST-ANGLE BOARD-BK4066?

The FDA product code for DELUXE ADJUST-ANGLE BOARD-BK4066 is ION.

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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: ION)

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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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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