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FDA 510(k)

ADD-ON TO CRITICAL PATIENT CARE BED

K-Number: K882177 · 1988-12-01

Decision Date1988-12-01
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ADD-ON TO CRITICAL PATIENT CARE BED is the device name listed in this FDA 510(k) record. The listed applicant is Cardio Systems, Inc.. It received FDA 510(k) clearance on 1988-12-01 under 510(k) number K882177. The device is classified under product code IOQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADD-ON TO CRITICAL PATIENT CARE BED?

ADD-ON TO CRITICAL PATIENT CARE BED is a medical device that received FDA 510(k) clearance on 1988-12-01. The listed applicant is Cardio Systems, Inc.. The 510(k) number is K882177.

When did ADD-ON TO CRITICAL PATIENT CARE BED receive FDA 510(k) clearance?

ADD-ON TO CRITICAL PATIENT CARE BED received FDA 510(k) clearance on 1988-12-01, under 510(k) number K882177.

Who is the listed applicant for ADD-ON TO CRITICAL PATIENT CARE BED?

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

What is the FDA product code for ADD-ON TO CRITICAL PATIENT CARE BED?

The FDA product code for ADD-ON TO CRITICAL PATIENT CARE BED is IOQ.

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.

Other records listing Cardio Systems, 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.

View all 9 devices →

Related Devices (Code: IOQ)

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.

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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