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FDA 510(k)

ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)

K-Number: K880647 · 1988-04-01

Decision Date1988-04-01
Product CodeHOX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ADULT PERCEPTUAL MOTOR PUZZLES (5331-01) 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 1988-04-01 under 510(k) number K880647. The device is classified under product code HOX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)?

ADULT PERCEPTUAL MOTOR PUZZLES (5331-01) is a medical device that received FDA 510(k) clearance on 1988-04-01. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K880647.

When did ADULT PERCEPTUAL MOTOR PUZZLES (5331-01) receive FDA 510(k) clearance?

ADULT PERCEPTUAL MOTOR PUZZLES (5331-01) received FDA 510(k) clearance on 1988-04-01, under 510(k) number K880647.

Who is the listed applicant for ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)?

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 ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)?

The FDA product code for ADULT PERCEPTUAL MOTOR PUZZLES (5331-01) is HOX.

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.

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.

View all 278 devices →

Related Devices (Code: HOX)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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