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FDA 510(k)

MAX-E-VAC

K-Number: K920217 · 1992-07-23

ApplicantLeisegang Medical, Inc.
Decision Date1992-07-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MAX-E-VAC is the device name listed in this FDA 510(k) record. The listed applicant is Leisegang Medical, Inc.. It received FDA 510(k) clearance on 1992-07-23 under 510(k) number K920217. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAX-E-VAC?

MAX-E-VAC is a medical device that received FDA 510(k) clearance on 1992-07-23. The listed applicant is Leisegang Medical, Inc.. The 510(k) number is K920217.

When did MAX-E-VAC receive FDA 510(k) clearance?

MAX-E-VAC received FDA 510(k) clearance on 1992-07-23, under 510(k) number K920217.

Who is the listed applicant for MAX-E-VAC?

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

What is the FDA product code for MAX-E-VAC?

The FDA product code for MAX-E-VAC is GEI.

Other records listing Leisegang Medical, 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.

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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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