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FDA 510(k)

AMBULATOR

K-Number: K921752 · 1992-05-04

ApplicantThe Anthros Medical Group
Decision Date1992-05-04
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AMBULATOR is the device name listed in this FDA 510(k) record. The listed applicant is The Anthros Medical Group. It received FDA 510(k) clearance on 1992-05-04 under 510(k) number K921752. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMBULATOR?

AMBULATOR is a medical device that received FDA 510(k) clearance on 1992-05-04. The listed applicant is The Anthros Medical Group. The 510(k) number is K921752.

When did AMBULATOR receive FDA 510(k) clearance?

AMBULATOR received FDA 510(k) clearance on 1992-05-04, under 510(k) number K921752.

Who is the listed applicant for AMBULATOR?

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

What is the FDA product code for AMBULATOR?

The FDA product code for AMBULATOR is INM.

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 The Anthros Medical Group 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.

K933060S-610 & 2-628 WHEELED SHOWER STRETCHERS

Related Devices (Code: INM)

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.

K063521NISSIN PEDIATRIC SERIES WHEELCHAIRNissin Medical, Inc.K941738STRYKER 5050 STRECHAIRStryker MedicalK941569CAREMOR CLINERWinco, Inc.K933000RECLINING GERI CHAIRS W/CASTERS & LAP TRAYWinco, Inc.K926028BENCHESTheradapt Products, Inc.K926054ELD-ARONDAK CHAIRAl'S Woodcraft, 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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