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FDA 510(k)

INFLATABLE PILLOW

K-Number: K823643 · 1983-02-03

ApplicantFred Sammons, Inc.
Decision Date1983-02-03
Product Code
DecisionSubstantially Equivalent

Device Summary

INFLATABLE PILLOW 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 1983-02-03 under 510(k) number K823643. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFLATABLE PILLOW?

INFLATABLE PILLOW is a medical device that received FDA 510(k) clearance on 1983-02-03. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K823643.

When did INFLATABLE PILLOW receive FDA 510(k) clearance?

INFLATABLE PILLOW received FDA 510(k) clearance on 1983-02-03, under 510(k) number K823643.

Who is the listed applicant for INFLATABLE PILLOW?

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

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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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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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