Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

COMPRESSOR, AIR, PORTABLE

K-Number: K813311 · 1981-12-31

ApplicantThe Biomed Group
Decision Date1981-12-31
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COMPRESSOR, AIR, PORTABLE is the device name listed in this FDA 510(k) record. The listed applicant is The Biomed Group. It received FDA 510(k) clearance on 1981-12-31 under 510(k) number K813311. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESSOR, AIR, PORTABLE?

COMPRESSOR, AIR, PORTABLE is a medical device that received FDA 510(k) clearance on 1981-12-31. The listed applicant is The Biomed Group. The 510(k) number is K813311.

When did COMPRESSOR, AIR, PORTABLE receive FDA 510(k) clearance?

COMPRESSOR, AIR, PORTABLE received FDA 510(k) clearance on 1981-12-31, under 510(k) number K813311.

Who is the listed applicant for COMPRESSOR, AIR, PORTABLE?

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

What is the FDA product code for COMPRESSOR, AIR, PORTABLE?

The FDA product code for COMPRESSOR, AIR, PORTABLE is BTI.

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 Biomed 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.

K810272BIO CARE OXYGEN CONCENTRATOR

Related Devices (Code: BTI)

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.

K131881OMBRA TABLE TOP COMPRESSORTrudell Medical Intl.K113338MEDICAL AIR COMPRESSOROricare, Inc.K091871DK50 DSEkom S.R.O.K072634EMG TRITON -COMP,MODEL NCA01-XXX SERIESEmg Technology Co., Ltd.K060781MEDICAL COMPRESSOR, MODELS DK50 D AND DMEkom S.R.O.K051691MINIMATE COMPRESSORPrecision Medical, 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.

↑