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FDA 510(k)

NEBULIZER PUMP, POWERED MODEL 1180

K-Number: K925011 · 1994-01-12

ApplicantThomas Industries
Decision Date1994-01-12
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER PUMP, POWERED MODEL 1180 is the device name listed in this FDA 510(k) record. The listed applicant is Thomas Industries. It received FDA 510(k) clearance on 1994-01-12 under 510(k) number K925011. 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 NEBULIZER PUMP, POWERED MODEL 1180?

NEBULIZER PUMP, POWERED MODEL 1180 is a medical device that received FDA 510(k) clearance on 1994-01-12. The listed applicant is Thomas Industries. The 510(k) number is K925011.

When did NEBULIZER PUMP, POWERED MODEL 1180 receive FDA 510(k) clearance?

NEBULIZER PUMP, POWERED MODEL 1180 received FDA 510(k) clearance on 1994-01-12, under 510(k) number K925011.

Who is the listed applicant for NEBULIZER PUMP, POWERED MODEL 1180?

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

What is the FDA product code for NEBULIZER PUMP, POWERED MODEL 1180?

The FDA product code for NEBULIZER PUMP, POWERED MODEL 1180 is BTI.

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Other records listing Thomas Industries 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.

K041199MEDI-PUMP ASPIRATOR, MODEL 1615K965059CPI, MAXI-VAC(6480),THOMAS INDUSTRIES, MEDI-PUMP(1240/1242/1243)K952806MEDI PUMP ASPIRATOR MODELS 1130 AND 1135K950290MEDI - PUMPK951729MEDI - PUMPK950867MEDI - PUMP

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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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