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FDA 510(k)

MEDIPAC II EC (TM), MODEL 7900

K-Number: K882820 · 1988-08-29

ApplicantMedical Devices, Inc.
Decision Date1988-08-29
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDIPAC II EC (TM), MODEL 7900 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1988-08-29 under 510(k) number K882820. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIPAC II EC (TM), MODEL 7900?

MEDIPAC II EC (TM), MODEL 7900 is a medical device that received FDA 510(k) clearance on 1988-08-29. The listed applicant is Medical Devices, Inc.. The 510(k) number is K882820.

When did MEDIPAC II EC (TM), MODEL 7900 receive FDA 510(k) clearance?

MEDIPAC II EC (TM), MODEL 7900 received FDA 510(k) clearance on 1988-08-29, under 510(k) number K882820.

Who is the listed applicant for MEDIPAC II EC (TM), MODEL 7900?

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

What is the FDA product code for MEDIPAC II EC (TM), MODEL 7900?

The FDA product code for MEDIPAC II EC (TM), MODEL 7900 is GZJ.

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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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