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FDA 510(k)

REGULATORS, HIGH SUCTION

K-Number: K760317 · 1976-08-04

ApplicantHarris-Lake, Inc.
Decision Date1976-08-04
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

REGULATORS, HIGH SUCTION is the device name listed in this FDA 510(k) record. The listed applicant is Harris-Lake, Inc.. It received FDA 510(k) clearance on 1976-08-04 under 510(k) number K760317. 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 REGULATORS, HIGH SUCTION?

REGULATORS, HIGH SUCTION is a medical device that received FDA 510(k) clearance on 1976-08-04. The listed applicant is Harris-Lake, Inc.. The 510(k) number is K760317.

When did REGULATORS, HIGH SUCTION receive FDA 510(k) clearance?

REGULATORS, HIGH SUCTION received FDA 510(k) clearance on 1976-08-04, under 510(k) number K760317.

Who is the listed applicant for REGULATORS, HIGH SUCTION?

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

What is the FDA product code for REGULATORS, HIGH SUCTION?

The FDA product code for REGULATORS, HIGH SUCTION is KDP.

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Other records listing Harris-Lake, 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.

K761293RESPIRATORY HUMIDIFIERK761294RESPIRATORY BLOWERK761295RESP. AIR TEMP. CONTROL & HAZARD MON.K760333JAR, COLLECTOR FOR SUCTION SYSTEMSK760314FLOWMETER, OXYGENK760316REGULATORS, LOW SUCTION

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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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