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FDA 510(k)

BOEHRINGER LAB SUCTION INTERRUPTER

K-Number: K853155 · 1985-10-16

ApplicantBoehringer Laboratories
Decision Date1985-10-16
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOEHRINGER LAB SUCTION INTERRUPTER is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1985-10-16 under 510(k) number K853155. 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 LAB SUCTION INTERRUPTER?

BOEHRINGER LAB SUCTION INTERRUPTER is a medical device that received FDA 510(k) clearance on 1985-10-16. The listed applicant is Boehringer Laboratories. The 510(k) number is K853155.

When did BOEHRINGER LAB SUCTION INTERRUPTER receive FDA 510(k) clearance?

BOEHRINGER LAB SUCTION INTERRUPTER received FDA 510(k) clearance on 1985-10-16, under 510(k) number K853155.

Who is the listed applicant for BOEHRINGER LAB SUCTION INTERRUPTER?

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 LAB SUCTION INTERRUPTER?

The FDA product code for BOEHRINGER LAB SUCTION INTERRUPTER is KDP.

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Other records listing Boehringer Laboratories as applicant

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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 LaboratoriesK926140VACUUM POWER BODY FLUID SUCTION APPARATUSHill-Rom, Inc.K922817PM3000 & PM3100 VACUUM REGULATORPrecision 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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