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FDA 510(k)

LAKE DISPOSABLE PROBE COVER

K-Number: K880578 · 1988-03-31

ApplicantLake Medical Products, Inc.
Decision Date1988-03-31
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LAKE DISPOSABLE PROBE COVER is the device name listed in this FDA 510(k) record. The listed applicant is Lake Medical Products, Inc.. It received FDA 510(k) clearance on 1988-03-31 under 510(k) number K880578. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAKE DISPOSABLE PROBE COVER?

LAKE DISPOSABLE PROBE COVER is a medical device that received FDA 510(k) clearance on 1988-03-31. The listed applicant is Lake Medical Products, Inc.. The 510(k) number is K880578.

When did LAKE DISPOSABLE PROBE COVER receive FDA 510(k) clearance?

LAKE DISPOSABLE PROBE COVER received FDA 510(k) clearance on 1988-03-31, under 510(k) number K880578.

Who is the listed applicant for LAKE DISPOSABLE PROBE COVER?

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

What is the FDA product code for LAKE DISPOSABLE PROBE COVER?

The FDA product code for LAKE DISPOSABLE PROBE COVER is FLL.

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Other records listing Lake Medical Products, Inc. as applicant

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Related Devices (Code: FLL)

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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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