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FDA 510(k)

DISCOVER(R)

K-Number: K882232 · 1988-10-25

ApplicantCarter Products
Decision Date1988-10-25
Product CodeLCX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DISCOVER(R) is the device name listed in this FDA 510(k) record. The listed applicant is Carter Products. It received FDA 510(k) clearance on 1988-10-25 under 510(k) number K882232. The device is classified under product code LCX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISCOVER(R)?

DISCOVER(R) is a medical device that received FDA 510(k) clearance on 1988-10-25. The listed applicant is Carter Products. The 510(k) number is K882232.

When did DISCOVER(R) receive FDA 510(k) clearance?

DISCOVER(R) received FDA 510(k) clearance on 1988-10-25, under 510(k) number K882232.

Who is the listed applicant for DISCOVER(R)?

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

What is the FDA product code for DISCOVER(R)?

The FDA product code for DISCOVER(R) is LCX.

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Related Devices (Code: LCX)

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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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