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FDA 510(k)

PARA-PAK SAF

K-Number: K792707 · 1980-01-21

Decision Date1980-01-21
Product CodeIGG
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

PARA-PAK SAF is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Diagnostics, Inc.. It received FDA 510(k) clearance on 1980-01-21 under 510(k) number K792707. The device is classified under product code IGG. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARA-PAK SAF?

PARA-PAK SAF is a medical device that received FDA 510(k) clearance on 1980-01-21. The listed applicant is Meridian Diagnostics, Inc.. The 510(k) number is K792707.

When did PARA-PAK SAF receive FDA 510(k) clearance?

PARA-PAK SAF received FDA 510(k) clearance on 1980-01-21, under 510(k) number K792707.

Who is the listed applicant for PARA-PAK SAF?

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

What is the FDA product code for PARA-PAK SAF?

The FDA product code for PARA-PAK SAF is IGG.

Other records listing Meridian Diagnostics, 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 92 devices →

Related Devices (Code: IGG)

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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