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FDA 510(k)

LAKE OSTOMY CARE SET

K-Number: K922730 · 1993-12-30

ApplicantLake Medical Products, Inc.
Decision Date1993-12-30
Product CodeEXB
Advisory CommitteeGU
DecisionUnknown

Device Summary

LAKE OSTOMY CARE SET 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 1993-12-30 under 510(k) number K922730. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the LAKE OSTOMY CARE SET?

LAKE OSTOMY CARE SET is a medical device that received FDA 510(k) clearance on 1993-12-30. The listed applicant is Lake Medical Products, Inc.. The 510(k) number is K922730.

When did LAKE OSTOMY CARE SET receive FDA 510(k) clearance?

LAKE OSTOMY CARE SET received FDA 510(k) clearance on 1993-12-30, under 510(k) number K922730.

Who is the listed applicant for LAKE OSTOMY CARE SET?

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 OSTOMY CARE SET?

The FDA product code for LAKE OSTOMY CARE SET is EXB.

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Other records listing Lake Medical Products, Inc. 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.

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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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