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FDA 510(k)

ANGEL WING SETS -- MODIFIED

K-Number: K922468 · 1992-07-10

ApplicantMbo Laboratories, Inc.
Decision Date1992-07-10
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANGEL WING SETS -- MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Mbo Laboratories, Inc.. It received FDA 510(k) clearance on 1992-07-10 under 510(k) number K922468. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGEL WING SETS -- MODIFIED?

ANGEL WING SETS -- MODIFIED is a medical device that received FDA 510(k) clearance on 1992-07-10. The listed applicant is Mbo Laboratories, Inc.. The 510(k) number is K922468.

When did ANGEL WING SETS -- MODIFIED receive FDA 510(k) clearance?

ANGEL WING SETS -- MODIFIED received FDA 510(k) clearance on 1992-07-10, under 510(k) number K922468.

Who is the listed applicant for ANGEL WING SETS -- MODIFIED?

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

What is the FDA product code for ANGEL WING SETS -- MODIFIED?

The FDA product code for ANGEL WING SETS -- MODIFIED is GIM.

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Other records listing Mbo Laboratories, 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.

K920184ANGEL WING SAFETY BLOOD COLLECTION WITH TUBE HOLD.K912563ANGEL WING SAFETY BLOOD COLLECTION AND INFUSION SE

Related Devices (Code: GIM)

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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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