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FDA 510(k)

MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER

K-Number: K903209 · 1990-12-21

ApplicantAdler Instrument Co.
Decision Date1990-12-21
Product CodeHES
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Adler Instrument Co.. It received FDA 510(k) clearance on 1990-12-21 under 510(k) number K903209. The device is classified under product code HES. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER?

MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER is a medical device that received FDA 510(k) clearance on 1990-12-21. The listed applicant is Adler Instrument Co.. The 510(k) number is K903209.

When did MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER receive FDA 510(k) clearance?

MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER received FDA 510(k) clearance on 1990-12-21, under 510(k) number K903209.

Who is the listed applicant for MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER?

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

What is the FDA product code for MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER?

The FDA product code for MAXI-FLOW INSUFFLATOR TUBING SET W/FILTER is HES.

Related Clinical Trials

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Other records listing Adler Instrument Co. 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.

K910170MAXI-FLOW SUCTION SET 12 FT.K910171MAXI-FLOW SUCTION SET W/Y CONNECTORK903208MAXI-FLOW INSUFFLATOR TUBING SETK900913ADLER DISPOSABLE BIPOLAR CORDK841723ADLER CUSTOM PROCEDURE PACKSK833264ADLER STEAM INDICATOR-GAS INDICATOR

View all 8 devices →

Related Devices (Code: HES)

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.

K000340HYSTALOG HSG CATHETERRocket Medical PlcK903208MAXI-FLOW INSUFFLATOR TUBING SETAdler Instrument Co.K904473KRONNER MANIPUJECTORUnimar, Inc.K901413CORE DISPOSABLE INSUFFLATION TUBINGCore Dynamics, Inc.K891290SHOLKOFF BALLOON HYSTEROSALPINGOGRAPHY CATHETERCook Ob/GynK890869BARD HYSTEROSALPINGOGRAPHY CATHETERSC.R. Bard, 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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