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FDA 510(k)

INFANT EVALUATION CARRIER

K-Number: K831731 · 1983-07-18

ApplicantE.M. Adams
Decision Date1983-07-18
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFANT EVALUATION CARRIER is the device name listed in this FDA 510(k) record. The listed applicant is E.M. Adams. It received FDA 510(k) clearance on 1983-07-18 under 510(k) number K831731. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFANT EVALUATION CARRIER?

INFANT EVALUATION CARRIER is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is E.M. Adams. The 510(k) number is K831731.

When did INFANT EVALUATION CARRIER receive FDA 510(k) clearance?

INFANT EVALUATION CARRIER received FDA 510(k) clearance on 1983-07-18, under 510(k) number K831731.

Who is the listed applicant for INFANT EVALUATION CARRIER?

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

What is the FDA product code for INFANT EVALUATION CARRIER?

The FDA product code for INFANT EVALUATION CARRIER is FPP.

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 E.M. Adams 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.

K905173SPLASH GUARDK910468STERILE DISPOSABLE DRAPE(S)K873978DISPOSABLE BIPOLAR FORCEPSK850063INSTRUMENT POCKETK843724I.V. START KIT & OBSTETRICAL KITK843783WET PACK

View all 21 devices →

Related Devices (Code: FPP)

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.

K030283BABY PODPrism Enterprises, Inc.K942356MED-EVAC-4 MEDICAL EVACUATION STRETCHERMontery Bay Corp.K940130STRYKER MODEL 6110 EMERGENCY/POLE STRETCHERStryker Corp.K940245EVACU-SLEDEvacu Technologies, Inc.K924275RESTRAINING STRETCHERDmsK922816U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIERUp Custom Design, 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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