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FDA 510(k)

AIRMED SMOKE EVACUATION & FILTER

K-Number: K820091 · 1982-02-24

ApplicantJames L. Geraci & Associates, Inc.
Decision Date1982-02-24
Product CodeCIE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AIRMED SMOKE EVACUATION & FILTER 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 1982-02-24 under 510(k) number K820091. The device is classified under product code CIE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIRMED SMOKE EVACUATION & FILTER?

AIRMED SMOKE EVACUATION & FILTER is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is James L. Geraci & Associates, Inc.. The 510(k) number is K820091.

When did AIRMED SMOKE EVACUATION & FILTER receive FDA 510(k) clearance?

AIRMED SMOKE EVACUATION & FILTER received FDA 510(k) clearance on 1982-02-24, under 510(k) number K820091.

Who is the listed applicant for AIRMED SMOKE EVACUATION & FILTER?

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 SMOKE EVACUATION & FILTER?

The FDA product code for AIRMED SMOKE EVACUATION & FILTER is CIE.

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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 IIK820079AIRMED PNEUMATIC EQUIP. FILTRA/CONTROLK820078DRAPE, SURGICALK811698CARL ZEISS INN MYRINGOTOMY TUBE LINE

Related Devices (Code: CIE)

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.

K904761P/N 35310, IL TEST ALKALINE PHOSPHATASE REAGENTInstrumentation Laboratory COK880967MICRO CO2 APPARATUSHf Scientific, Inc.K864313CO2 REAGENT SETHf Scientific, Inc.K832071TOTAL CO2 REAGENT SETAmerican Research Products Co.K800524SERALYZER REFLECTANCE PHOTOMETER/CALIB.Miles Laboratories, Inc.K771610CARBON DIOXIDE ANALYZERCorning Medical & Scientific

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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