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FDA 510(k)

AIR PLETHYSMOGRAPH MODEL APG-1000

K-Number: K881291 · 1988-10-14

ApplicantAci Medical, Inc.
Decision Date1988-10-14
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AIR PLETHYSMOGRAPH MODEL APG-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Aci Medical, Inc.. It received FDA 510(k) clearance on 1988-10-14 under 510(k) number K881291. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIR PLETHYSMOGRAPH MODEL APG-1000?

AIR PLETHYSMOGRAPH MODEL APG-1000 is a medical device that received FDA 510(k) clearance on 1988-10-14. The listed applicant is Aci Medical, Inc.. The 510(k) number is K881291.

When did AIR PLETHYSMOGRAPH MODEL APG-1000 receive FDA 510(k) clearance?

AIR PLETHYSMOGRAPH MODEL APG-1000 received FDA 510(k) clearance on 1988-10-14, under 510(k) number K881291.

Who is the listed applicant for AIR PLETHYSMOGRAPH MODEL APG-1000?

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

What is the FDA product code for AIR PLETHYSMOGRAPH MODEL APG-1000?

The FDA product code for AIR PLETHYSMOGRAPH MODEL APG-1000 is DSB.

Related Clinical Trials

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Other records listing Aci Medical, 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.

K942530ART-ASSIST MODEL AA-1000K903894VENAPULSE MODELS VP-25 AND VP-50K903532UNNA-SLEEVE(TM)K861645MICRO-TRACHEOSTOMY CARE KITK844309IV RATEMETER

Related Devices (Code: DSB)

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.

K260224MySOZO Software version 6.1.0.1 (SW version 6.1.0.1)ImpediMed LimitedK250634BCM2-Body Composition MonitorFresenius Medical Care Renal Therapies Group, LLCK243727Re:BalansMode Sensors ASK250922Edema Guard Monitor (EGM) CardioSet-001Cardioset Medical , Ltd.K232089SOZO ProImpediMed LimitedK223217Zynex Monitoring System, Model CM-1600Zynex Medical, 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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