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FDA 510(k)

AIA-PACK BMG

K-Number: K900440 · 1990-02-26

Decision Date1990-02-26
Product CodeJZG
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

AIA-PACK BMG is the device name listed in this FDA 510(k) record. The listed applicant is Tosoh Medics, Inc.. It received FDA 510(k) clearance on 1990-02-26 under 510(k) number K900440. The device is classified under product code JZG. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIA-PACK BMG?

AIA-PACK BMG is a medical device that received FDA 510(k) clearance on 1990-02-26. The listed applicant is Tosoh Medics, Inc.. The 510(k) number is K900440.

When did AIA-PACK BMG receive FDA 510(k) clearance?

AIA-PACK BMG received FDA 510(k) clearance on 1990-02-26, under 510(k) number K900440.

Who is the listed applicant for AIA-PACK BMG?

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

What is the FDA product code for AIA-PACK BMG?

The FDA product code for AIA-PACK BMG is JZG.

Other records listing Tosoh Medics, 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.

View all 41 devices →

Related Devices (Code: JZG)

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.

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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