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FDA 510(k)

CRASH CART

K-Number: K832355 · 1983-10-28

ApplicantQuinton, Inc.
Decision Date1983-10-28
Product CodeBZN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CRASH CART is the device name listed in this FDA 510(k) record. The listed applicant is Quinton, Inc.. It received FDA 510(k) clearance on 1983-10-28 under 510(k) number K832355. The device is classified under product code BZN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRASH CART?

CRASH CART is a medical device that received FDA 510(k) clearance on 1983-10-28. The listed applicant is Quinton, Inc.. The 510(k) number is K832355.

When did CRASH CART receive FDA 510(k) clearance?

CRASH CART received FDA 510(k) clearance on 1983-10-28, under 510(k) number K832355.

Who is the listed applicant for CRASH CART?

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

What is the FDA product code for CRASH CART?

The FDA product code for CRASH CART is BZN.

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.

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Other records listing Quinton, 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.

K032038PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601K021906QUINTON Q-CATH, MODEL 000460K003576Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503K001492QUINTON Q-STRESS, MODEL 000483K992908Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)K990866QUINTON MEDTRACK CR PLUS TREADMILL

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Related Devices (Code: BZN)

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.

K924373ACCUFLATE ACCESSORIE CART W/IV POLE AND CLAMPInstrumed, Inc.K872558CART, EMERGENCY, CARDIOPULMONARYNico Metal Products Corp.K850761MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY CMedicor USA , Ltd.K840264SERVO CART 170Siemens Elema ABK832697RMP INTUBATION EQUIP. STORAGE TRAYRmp Co.K832356PORTABLE OPERAT. RM. MONITORS HS30/40Medtel Pty. , Ltd.

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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