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FDA 510(k)

POCKET AID

K-Number: K832702 · 1983-11-17

ApplicantM.C. Johnson Co., Inc.
Decision Date1983-11-17
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POCKET AID is the device name listed in this FDA 510(k) record. The listed applicant is M.C. Johnson Co., Inc.. It received FDA 510(k) clearance on 1983-11-17 under 510(k) number K832702. The device is classified under product code LDR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POCKET AID?

POCKET AID is a medical device that received FDA 510(k) clearance on 1983-11-17. The listed applicant is M.C. Johnson Co., Inc.. The 510(k) number is K832702.

When did POCKET AID receive FDA 510(k) clearance?

POCKET AID received FDA 510(k) clearance on 1983-11-17, under 510(k) number K832702.

Who is the listed applicant for POCKET AID?

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

What is the FDA product code for POCKET AID?

The FDA product code for POCKET AID is LDR.

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.

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Other records listing M.C. Johnson Co., 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.

K953375NG SECUREK872525A.L.A.R.M. (ADJUST. LEG & ANKLE REPOSITIONING MECH

Related Devices (Code: LDR)

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.

K242693DEKA Infusion System, DEKA Administration SetDeka Research and Development CorporationK232316DEKA Infusion System, DEKA Administration SetDeka Research and DevelopmentK153760Volumetric Infusion ControllerDEKA Research & DevelopmentK963136PACER MODEL 100 INFUSION CONTROLLERHealth Watch, Inc.K971826ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500Alexander Mfg. Co.K971865ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3PAlexander Mfg. 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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