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FDA 510(k)

GINGERBREAD MAN (TM)

K-Number: K862093 · 1986-07-22

ApplicantSouthern Pride Manufacturing, Inc.
Decision Date1986-07-22
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GINGERBREAD MAN (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Southern Pride Manufacturing, Inc.. It received FDA 510(k) clearance on 1986-07-22 under 510(k) number K862093. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GINGERBREAD MAN (TM)?

GINGERBREAD MAN (TM) is a medical device that received FDA 510(k) clearance on 1986-07-22. The listed applicant is Southern Pride Manufacturing, Inc.. The 510(k) number is K862093.

When did GINGERBREAD MAN (TM) receive FDA 510(k) clearance?

GINGERBREAD MAN (TM) received FDA 510(k) clearance on 1986-07-22, under 510(k) number K862093.

Who is the listed applicant for GINGERBREAD MAN (TM)?

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

What is the FDA product code for GINGERBREAD MAN (TM)?

The FDA product code for GINGERBREAD MAN (TM) is BXB.

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Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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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