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FDA 510(k)

VACUUM POWER BODY FLUID SUCTION APPARATUS

K-Number: K926140 · 1993-07-27

ApplicantHill-Rom, Inc.
Decision Date1993-07-27
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VACUUM POWER BODY FLUID SUCTION APPARATUS is the device name listed in this FDA 510(k) record. The listed applicant is Hill-Rom, Inc.. It received FDA 510(k) clearance on 1993-07-27 under 510(k) number K926140. The device is classified under product code KDP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUUM POWER BODY FLUID SUCTION APPARATUS?

VACUUM POWER BODY FLUID SUCTION APPARATUS is a medical device that received FDA 510(k) clearance on 1993-07-27. The listed applicant is Hill-Rom, Inc.. The 510(k) number is K926140.

When did VACUUM POWER BODY FLUID SUCTION APPARATUS receive FDA 510(k) clearance?

VACUUM POWER BODY FLUID SUCTION APPARATUS received FDA 510(k) clearance on 1993-07-27, under 510(k) number K926140.

Who is the listed applicant for VACUUM POWER BODY FLUID SUCTION APPARATUS?

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

What is the FDA product code for VACUUM POWER BODY FLUID SUCTION APPARATUS?

The FDA product code for VACUUM POWER BODY FLUID SUCTION APPARATUS is KDP.

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Other records listing Hill-Rom, 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.

K260211Dashboard (P007000)K202018Hill-Rom Heart and Respiration Rate Monitoring System: Single Sensor, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Packs, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor ActivationK180079Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor Packs (different #), Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor ActivationK013709HILL-ROM PRIMAVIEW MONITOR SYSTEMK973705CONTOR TABLE SURFACEK981081BRIGHTSTAR

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Related Devices (Code: KDP)

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.

K013976BOEHRINGER MRI SUCTION REGULATORYBoehringer LaboratoriesK944479PM3300 INTERMITTENT VACUUMPrecision Medical, Inc.K942747MALCOLM-LYNN(TM) EOT SUCTION REG VALVE(TM) (SRV) )Engineered Orthopedic Technologies, Inc.K933232BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIEDBoehringer LaboratoriesK922817PM3000 & PM3100 VACUUM REGULATORPrecision Medical, Inc.K883229OHMEDA CONTINUOUS SUCTION REGULATOROhmeda Medical

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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