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FDA 510(k)

SNIFF POSITION PILLOW

K-Number: K934235 · 1993-10-01

ApplicantAmerican Medical Development, Inc.
Decision Date1993-10-01
Product CodeCCX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SNIFF POSITION PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Development, Inc.. It received FDA 510(k) clearance on 1993-10-01 under 510(k) number K934235. The device is classified under product code CCX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNIFF POSITION PILLOW?

SNIFF POSITION PILLOW is a medical device that received FDA 510(k) clearance on 1993-10-01. The listed applicant is American Medical Development, Inc.. The 510(k) number is K934235.

When did SNIFF POSITION PILLOW receive FDA 510(k) clearance?

SNIFF POSITION PILLOW received FDA 510(k) clearance on 1993-10-01, under 510(k) number K934235.

Who is the listed applicant for SNIFF POSITION PILLOW?

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

What is the FDA product code for SNIFF POSITION PILLOW?

The FDA product code for SNIFF POSITION PILLOW is CCX.

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Related Devices (Code: CCX)

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.

K943837CHIN UPEdward CardenK932305VILA-COOKE(TM) ANESTHESIA PILLOWSharn, Inc.K861915SURGICAL HEAD SUPPORTTreace Medical, Inc.K833022AIR UTERINE DISPLACER-AUD 120Scientific Sales Intl., Inc.K821838VARI-SUPPORT LOW BACK POSTURE PILLOWBody Therapeutics, Inc.K810035PRENATAL SUPPORT PILLOWSupportech, Inc.

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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