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FDA 510(k)

BOEHRINGER MRI SUCTION REGULATORY

K-Number: K013976 · 2002-01-08

ApplicantBoehringer Laboratories
Decision Date2002-01-08
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOEHRINGER MRI SUCTION REGULATORY is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 2002-01-08 under 510(k) number K013976. 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 BOEHRINGER MRI SUCTION REGULATORY?

BOEHRINGER MRI SUCTION REGULATORY is a medical device that received FDA 510(k) clearance on 2002-01-08. The listed applicant is Boehringer Laboratories. The 510(k) number is K013976.

When did BOEHRINGER MRI SUCTION REGULATORY receive FDA 510(k) clearance?

BOEHRINGER MRI SUCTION REGULATORY received FDA 510(k) clearance on 2002-01-08, under 510(k) number K013976.

Who is the listed applicant for BOEHRINGER MRI SUCTION REGULATORY?

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

What is the FDA product code for BOEHRINGER MRI SUCTION REGULATORY?

The FDA product code for BOEHRINGER MRI SUCTION REGULATORY is KDP.

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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.

K944479PM3300 INTERMITTENT VACUUMPrecision Medical, Inc.K942747MALCOLM-LYNN(TM) EOT SUCTION REG VALVE(TM) (SRV) )Engineered Orthopedic Technologies, Inc.K933232BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIEDBoehringer LaboratoriesK926140VACUUM POWER BODY FLUID SUCTION APPARATUSHill-Rom, Inc.K922817PM3000 & 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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