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FDA 510(k)

PRENATAL SUPPORT PILLOW

K-Number: K810035 · 1981-01-23

ApplicantSupportech, Inc.
Decision Date1981-01-23
Product CodeCCX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRENATAL SUPPORT PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Supportech, Inc.. It received FDA 510(k) clearance on 1981-01-23 under 510(k) number K810035. 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 PRENATAL SUPPORT PILLOW?

PRENATAL SUPPORT PILLOW is a medical device that received FDA 510(k) clearance on 1981-01-23. The listed applicant is Supportech, Inc.. The 510(k) number is K810035.

When did PRENATAL SUPPORT PILLOW receive FDA 510(k) clearance?

PRENATAL SUPPORT PILLOW received FDA 510(k) clearance on 1981-01-23, under 510(k) number K810035.

Who is the listed applicant for PRENATAL SUPPORT PILLOW?

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

What is the FDA product code for PRENATAL SUPPORT PILLOW?

The FDA product code for PRENATAL SUPPORT PILLOW is CCX.

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.

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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.K934235SNIFF POSITION PILLOWAmerican Medical Development, Inc.K861915SURGICAL HEAD SUPPORTTreace Medical, Inc.K833022AIR UTERINE DISPLACER-AUD 120Scientific Sales Intl., Inc.K821838VARI-SUPPORT LOW BACK POSTURE PILLOWBody Therapeutics, Inc.

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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