ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)
K-Number: K880647 · 1988-04-01
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Device Summary
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.
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
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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