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FDA 510(k)

ENDOCATER

K-Number: K863393 · 1987-06-11

ApplicantThe Hygenic Corp.
Decision Date1987-06-11
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

ENDOCATER is the device name listed in this FDA 510(k) record. The listed applicant is The Hygenic Corp.. It received FDA 510(k) clearance on 1987-06-11 under 510(k) number K863393. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOCATER?

ENDOCATER is a medical device that received FDA 510(k) clearance on 1987-06-11. The listed applicant is The Hygenic Corp.. The 510(k) number is K863393.

When did ENDOCATER receive FDA 510(k) clearance?

ENDOCATER received FDA 510(k) clearance on 1987-06-11, under 510(k) number K863393.

Who is the listed applicant for ENDOCATER?

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

What is the FDA product code for ENDOCATER?

The FDA product code for ENDOCATER is LQY.

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Other records listing The Hygenic Corp. as applicant

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Related Devices (Code: LQY)

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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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