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FDA 510(k)

FERRIS ECG ELECTRODE W/HYDROGEL

K-Number: K873682 · 1987-12-29

ApplicantFerris Mfg. Corp.
Decision Date1987-12-29
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FERRIS ECG ELECTRODE W/HYDROGEL is the device name listed in this FDA 510(k) record. The listed applicant is Ferris Mfg. Corp.. It received FDA 510(k) clearance on 1987-12-29 under 510(k) number K873682. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FERRIS ECG ELECTRODE W/HYDROGEL?

FERRIS ECG ELECTRODE W/HYDROGEL is a medical device that received FDA 510(k) clearance on 1987-12-29. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K873682.

When did FERRIS ECG ELECTRODE W/HYDROGEL receive FDA 510(k) clearance?

FERRIS ECG ELECTRODE W/HYDROGEL received FDA 510(k) clearance on 1987-12-29, under 510(k) number K873682.

Who is the listed applicant for FERRIS ECG ELECTRODE W/HYDROGEL?

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

What is the FDA product code for FERRIS ECG ELECTRODE W/HYDROGEL?

The FDA product code for FERRIS ECG ELECTRODE W/HYDROGEL is DRX.

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Other records listing Ferris Mfg. Corp. 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.

K031660FERRIS POLYMEM STERILE BREAST PADK031307FERRIS POLYMEM SILVER WOUND DRESSINGK002129FERRIS POLYMEM STERILE WOUND DRESSING WITH COLLAGENK991729FERRIS POLYOSTOMY STERILE WOUND DRESSINGK990906FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLERK984539FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSING

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Related Devices (Code: DRX)

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.

K171244PhysiotraceNimbleheart, Inc.K123658BIOMODULE 3-M1Zephyr Technology CorporationK101576CENTERRIDGE DIAGNOSTIC ECG ELECTRODE, CENTERRIDGE MONITORING ECG ELECTRODESTeam Innovations, Inc.K101685IP-SETIntegral Process SasK100129AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO XAmbu A/SK093327INTCO TAB ELECTRODEShanghai Intco Electrode Manufacturing Co., Ltd.

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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