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FDA 510(k)

BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED

K-Number: K933232 · 1994-03-28

ApplicantBoehringer Laboratories
Decision Date1994-03-28
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1994-03-28 under 510(k) number K933232. 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 LABORATORIES SUCTION REGULATOR, MODIFIED?

BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED is a medical device that received FDA 510(k) clearance on 1994-03-28. The listed applicant is Boehringer Laboratories. The 510(k) number is K933232.

When did BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED receive FDA 510(k) clearance?

BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED received FDA 510(k) clearance on 1994-03-28, under 510(k) number K933232.

Who is the listed applicant for BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED?

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 LABORATORIES SUCTION REGULATOR, MODIFIED?

The FDA product code for BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED is KDP.

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Other records listing Boehringer Laboratories 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.

K234145ViSiGi 3D Gastric Sizing TubeK061788BOEHRINGER LABORATORIES SUCTION PUMP SYSTEMK060277BOEHRINGER LABORATORIES SUCTION PUMP SYSTEMK020538BOEHRINGER LABORATORIES PNEUMATIC AMBULATORY COMPRESSION SYSTEM 8200 SERIESK014187AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEMK013976BOEHRINGER MRI SUCTION REGULATORY

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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.K926140VACUUM 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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