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FDA 510(k)

MODIFIED CHICK AMBULATORY HALO

K-Number: K884242 · 1988-12-29

ApplicantChick Medical Products
Decision Date1988-12-29
Product CodeJEC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFIED CHICK AMBULATORY HALO is the device name listed in this FDA 510(k) record. The listed applicant is Chick Medical Products. It received FDA 510(k) clearance on 1988-12-29 under 510(k) number K884242. The device is classified under product code JEC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED CHICK AMBULATORY HALO?

MODIFIED CHICK AMBULATORY HALO is a medical device that received FDA 510(k) clearance on 1988-12-29. The listed applicant is Chick Medical Products. The 510(k) number is K884242.

When did MODIFIED CHICK AMBULATORY HALO receive FDA 510(k) clearance?

MODIFIED CHICK AMBULATORY HALO received FDA 510(k) clearance on 1988-12-29, under 510(k) number K884242.

Who is the listed applicant for MODIFIED CHICK AMBULATORY HALO?

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

What is the FDA product code for MODIFIED CHICK AMBULATORY HALO?

The FDA product code for MODIFIED CHICK AMBULATORY HALO is JEC.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Chick Medical Products 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.

K901830CHICK III SURGICAL LIGHTING SYSTEM

Related Devices (Code: JEC)

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.

K203605SteriTrakArbutus Medical, Inc.K193256Anjon Bremer Halo SystemAnjon Holdings, LLCK192465DigiFix Sterile KitVirak Orthopedics, LLCK181192PIP FixHand Biomechanics Lab, Inc.K171863Anjon Bremer Halo SystemAnjon Holdings, LLCK163028Medline ReNewal Reprocessed Stryker External Fixation DevicesSurgical Instrument Service and Savings, 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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