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FDA 510(k)

AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL

K-Number: K820079 · 1982-02-05

ApplicantJames L. Geraci & Associates, Inc.
Decision Date1982-02-05
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is James L. Geraci & Associates, Inc.. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K820079. 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 AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL?

AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is James L. Geraci & Associates, Inc.. The 510(k) number is K820079.

When did AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL receive FDA 510(k) clearance?

AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL received FDA 510(k) clearance on 1982-02-05, under 510(k) number K820079.

Who is the listed applicant for AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL?

The FDA 510(k) record lists James L. Geraci & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL?

The FDA product code for AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL is BTI.

Related Clinical Trials

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Other records listing James L. Geraci & Associates, 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.

K853927LASE SYSTEM IIK820091AIRMED SMOKE EVACUATION & FILTERK820078DRAPE, SURGICALK811698CARL ZEISS INN MYRINGOTOMY TUBE LINE

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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