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FDA 510(k)

ADJUST. WEIGHTS-BK5171-05,10,20 BEOK

K-Number: K831543 · 1983-06-24

ApplicantFred Sammons, Inc.
Decision Date1983-06-24
Product CodeION
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ADJUST. WEIGHTS-BK5171-05,10,20 BEOK 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 1983-06-24 under 510(k) number K831543. 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 ADJUST. WEIGHTS-BK5171-05,10,20 BEOK?

ADJUST. WEIGHTS-BK5171-05,10,20 BEOK is a medical device that received FDA 510(k) clearance on 1983-06-24. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K831543.

When did ADJUST. WEIGHTS-BK5171-05,10,20 BEOK receive FDA 510(k) clearance?

ADJUST. WEIGHTS-BK5171-05,10,20 BEOK received FDA 510(k) clearance on 1983-06-24, under 510(k) number K831543.

Who is the listed applicant for ADJUST. WEIGHTS-BK5171-05,10,20 BEOK?

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 ADJUST. WEIGHTS-BK5171-05,10,20 BEOK?

The FDA product code for ADJUST. WEIGHTS-BK5171-05,10,20 BEOK is ION.

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Other records listing Fred Sammons, Inc. as applicant

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Related Devices (Code: ION)

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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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