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Adler Instrument Company

Brooksville, FL, US

ADLER INSTRUMENT COMPANY appears in FDA device records in Brooksville, FL. FDA records list 8 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
8
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 8 510(k) clearances for Adler Instrument Company between 1983 and 1991. The busiest year on record is 1990, with 3. The most recent is 1991, with 2.

Clearances by year, as a table
510(k) clearance decisions for Adler Instrument Company, by decision year
YearClearances
19832
19841
19903
19912
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K910171MAXI-FLOW SUCTION SET W/Y CONNECTORGAZSubstantially Equivalent
K910170MAXI-FLOW SUCTION SET 12 FT.GAZSubstantially Equivalent
K903209MAXI-FLOW INSUFFLATOR TUBING SET W/FILTERHESSubstantially Equivalent
K903208MAXI-FLOW INSUFFLATOR TUBING SETHESSubstantially Equivalent
K900913ADLER DISPOSABLE BIPOLAR CORDHQOSubstantially Equivalent
K841723ADLER CUSTOM PROCEDURE PACKSSubstantially Equivalent
K833264ADLER STEAM INDICATOR-GAS INDICATORJOJSubstantially Equivalent
K831068CONTAINER SYSTEMSubstantially Equivalent

Registered establishments

FDA registered establishments for Adler Instrument Company, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30075079733010034765ADLER INSTRUMENT COMPANY16460 Cortez Blvd, Brooksville, FL 34601 US2026and 71 more, listed in full below

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain