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FDA 510(k)

VARIOUS CAMEO MED PERCUTANEOUS SKIN PREP TRAYS,

K-Number: K922961 · 1993-03-23

ApplicantCameo, Inc.
Decision Date1993-03-23
Product CodeKKX
Advisory CommitteeSU
DecisionUnknown

Device Summary

VARIOUS CAMEO MED PERCUTANEOUS SKIN PREP TRAYS, is the device name listed in this FDA 510(k) record. The listed applicant is Cameo, Inc.. It received FDA 510(k) clearance on 1993-03-23 under 510(k) number K922961. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VARIOUS CAMEO MED PERCUTANEOUS SKIN PREP TRAYS,?

VARIOUS CAMEO MED PERCUTANEOUS SKIN PREP TRAYS, is a medical device that received FDA 510(k) clearance on 1993-03-23. The listed applicant is Cameo, Inc.. The 510(k) number is K922961.

When did VARIOUS CAMEO MED PERCUTANEOUS SKIN PREP TRAYS, receive FDA 510(k) clearance?

VARIOUS CAMEO MED PERCUTANEOUS SKIN PREP TRAYS, received FDA 510(k) clearance on 1993-03-23, under 510(k) number K922961.

Who is the listed applicant for VARIOUS CAMEO MED PERCUTANEOUS SKIN PREP TRAYS,?

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

What is the FDA product code for VARIOUS CAMEO MED PERCUTANEOUS SKIN PREP TRAYS,?

The FDA product code for VARIOUS CAMEO MED PERCUTANEOUS SKIN PREP TRAYS, is KKX.

Related Clinical Trials

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.

Other records listing Cameo, 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.

Related Devices (Code: KKX)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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