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FDA 510(k)

MAXI-VAC TM

K-Number: K790763 · 1979-04-23

ApplicantMed General
Decision Date1979-04-23
Product CodeGCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MAXI-VAC TM is the device name listed in this FDA 510(k) record. The listed applicant is Med General. It received FDA 510(k) clearance on 1979-04-23 under 510(k) number K790763. The device is classified under product code GCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXI-VAC TM?

MAXI-VAC TM is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Med General. The 510(k) number is K790763.

When did MAXI-VAC TM receive FDA 510(k) clearance?

MAXI-VAC TM received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790763.

Who is the listed applicant for MAXI-VAC TM?

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

What is the FDA product code for MAXI-VAC TM?

The FDA product code for MAXI-VAC TM is GCY.

Other records listing Med General 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.

K791097CEPTORTRODE WITH CEPTOR HESIVEK791098SINGLE-USE MINI-BULLDOGK790269CEPTOR HESIVEK782006MEDGENERAL SINGLE-USE BULLDOGK781239MYO-STIMK780632MAXICEPTOR

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Related Devices (Code: GCY)

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.

K972703REDYROB-CLOSED WOUND DRAINAGE SYSTEMB.Braun Medical, Inc.K971036ODONTIT AUTOGENOUS BONE COLLECTION DEVICEInterpore Intl.K963839CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500Cordis Corp.K960099PENROSE DRAIN MODELS 6001 - 6007Sil-Med Corp.K950754MACRO SUCTION TUBE MODEL NO 10061Dlp, Inc.K936223PRESSURE IRRIGATING SYSTEMLevel 1 Technologies, Inc.

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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