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FDA 510(k)

RESPIRATORY BLOWER

K-Number: K761294 · 1977-01-03

ApplicantHarris-Lake, Inc.
Decision Date1977-01-03
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRATORY BLOWER 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 1977-01-03 under 510(k) number K761294. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRATORY BLOWER?

RESPIRATORY BLOWER is a medical device that received FDA 510(k) clearance on 1977-01-03. The listed applicant is Harris-Lake, Inc.. The 510(k) number is K761294.

When did RESPIRATORY BLOWER receive FDA 510(k) clearance?

RESPIRATORY BLOWER received FDA 510(k) clearance on 1977-01-03, under 510(k) number K761294.

Who is the listed applicant for RESPIRATORY BLOWER?

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 RESPIRATORY BLOWER?

The FDA product code for RESPIRATORY BLOWER is BTI.

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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 HUMIDIFIERK761295RESP. AIR TEMP. CONTROL & HAZARD MON.K760333JAR, COLLECTOR FOR SUCTION SYSTEMSK760317REGULATORS, HIGH SUCTIONK760314FLOWMETER, OXYGENK760316REGULATORS, LOW SUCTION

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Related Devices (Code: BTI)

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.

K131881OMBRA TABLE TOP COMPRESSORTrudell Medical Intl.K113338MEDICAL AIR COMPRESSOROricare, Inc.K091871DK50 DSEkom S.R.O.K072634EMG TRITON -COMP,MODEL NCA01-XXX SERIESEmg Technology Co., Ltd.K060781MEDICAL COMPRESSOR, MODELS DK50 D AND DMEkom S.R.O.K051691MINIMATE COMPRESSORPrecision 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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