FDA 510(k)

RIKEN GAS INDICATOR (3 MODELS, 1806H, 1802D, IF-18)

K-Number: K951366 · 1995-08-02

Decision Date1995-08-02

Product CodeCBS

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

RIKEN GAS INDICATOR (3 MODELS, 1806H, 1802D, IF-18) is the device name listed in this FDA 510(k) record. The listed applicant is Riken Keiki Co., Ltd.. It received FDA 510(k) clearance on 1995-08-02 under 510(k) number K951366. The device is classified under product code CBS. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIKEN GAS INDICATOR (3 MODELS, 1806H, 1802D, IF-18)?

RIKEN GAS INDICATOR (3 MODELS, 1806H, 1802D, IF-18) is a medical device that received FDA 510(k) clearance on 1995-08-02. The listed applicant is Riken Keiki Co., Ltd.. The 510(k) number is K951366.

When did RIKEN GAS INDICATOR (3 MODELS, 1806H, 1802D, IF-18) receive FDA 510(k) clearance?

RIKEN GAS INDICATOR (3 MODELS, 1806H, 1802D, IF-18) received FDA 510(k) clearance on 1995-08-02, under 510(k) number K951366.

Who is the listed applicant for RIKEN GAS INDICATOR (3 MODELS, 1806H, 1802D, IF-18)?

The FDA 510(k) record lists Riken Keiki Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIKEN GAS INDICATOR (3 MODELS, 1806H, 1802D, IF-18)?

The FDA product code for RIKEN GAS INDICATOR (3 MODELS, 1806H, 1802D, IF-18) is CBS.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: CBS)

K974903GAS MODULE II, MODEL 0998-00-0143Datascope Corp.K953795VITALMAX 4100Pace Tech, Inc.K960490AS/3 COMPACT AIRWAY MODULE M-CAIOVDatex Medical Instrumentation, Inc.K950101RAMS (RANDOM ACCESS MASS SPECTROMETER) M-200 RESPIRATORY GAS MONITORMarquette Electronics, Inc.K943458AS/3 AIRWAY MODULEDatex Division Instrumentarium Corp.K942737POET IQ WITH FIVE AGENT CAPABILITYCriticare Systems, 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.