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)

CAM-10 CUIRASS SHELL

K-Number: K792673 · 1980-01-11

ApplicantLifecare Services, Inc.
Decision Date1980-01-11
Product CodeBYT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAM-10 CUIRASS SHELL is the device name listed in this FDA 510(k) record. The listed applicant is Lifecare Services, Inc.. It received FDA 510(k) clearance on 1980-01-11 under 510(k) number K792673. The device is classified under product code BYT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAM-10 CUIRASS SHELL?

CAM-10 CUIRASS SHELL is a medical device that received FDA 510(k) clearance on 1980-01-11. The listed applicant is Lifecare Services, Inc.. The 510(k) number is K792673.

When did CAM-10 CUIRASS SHELL receive FDA 510(k) clearance?

CAM-10 CUIRASS SHELL received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792673.

Who is the listed applicant for CAM-10 CUIRASS SHELL?

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

What is the FDA product code for CAM-10 CUIRASS SHELL?

The FDA product code for CAM-10 CUIRASS SHELL is BYT.

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 Lifecare Services, Inc. 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.

K913423LIFECARE REMOTE ALARM IIK912224LIFECARE CPAP-100K910947NEV-10 NEGATIVE PRESSURE VENTILATORK894779LIFECARE NASAL MASK KIT CAT. NO. 06-800K895592FREEWAY NEBULIZER COMPRESSORK894361LIFECARE PRESSURE ALARM CAT. NO. 34-010

View all 20 devices →

Related Devices (Code: BYT)

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.

K082657RTX RESPIRATORMedivent LimitedK072290PEGASO V, NEGAVENT RESPIRATOR, MODEL: DA-3 PLUSDima Italia SrlK924341HAYEK OSCILLATOR(TM)Respironics, Inc.K910947NEV-10 NEGATIVE PRESSURE VENTILATORLifecare Services, Inc.K905530PURITAN-BENNETT COMPANION 500 LIQUID OXYGEN SYSTEMPuritan Bennett Corp.K902764EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARMJ. H. Emerson Co.

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.

↑