FDA 510(k)

CHIN UP

K-Number: K943837 · 1994-10-14

Decision Date1994-10-14

Product CodeCCX

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

CHIN UP is the device name listed in this FDA 510(k) record. The listed applicant is Edward Carden. It received FDA 510(k) clearance on 1994-10-14 under 510(k) number K943837. 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 CHIN UP?

CHIN UP is a medical device that received FDA 510(k) clearance on 1994-10-14. The listed applicant is Edward Carden. The 510(k) number is K943837.

When did CHIN UP receive FDA 510(k) clearance?

CHIN UP received FDA 510(k) clearance on 1994-10-14, under 510(k) number K943837.

Who is the listed applicant for CHIN UP?

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

What is the FDA product code for CHIN UP?

The FDA product code for CHIN UP is CCX.

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.

K932305VILA-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.K810035PRENATAL SUPPORT PILLOWSupportech, 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.