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FDA 510(k)

ADULT ZEE-FRAME

K-Number: K790410 · 1979-03-22

Decision Date1979-03-22
Product CodeJAY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ADULT ZEE-FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Equilibrated Bio Systems, Inc.. It received FDA 510(k) clearance on 1979-03-22 under 510(k) number K790410. The device is classified under product code JAY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADULT ZEE-FRAME?

ADULT ZEE-FRAME is a medical device that received FDA 510(k) clearance on 1979-03-22. The listed applicant is Equilibrated Bio Systems, Inc.. The 510(k) number is K790410.

When did ADULT ZEE-FRAME receive FDA 510(k) clearance?

ADULT ZEE-FRAME received FDA 510(k) clearance on 1979-03-22, under 510(k) number K790410.

Who is the listed applicant for ADULT ZEE-FRAME?

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

What is the FDA product code for ADULT ZEE-FRAME?

The FDA product code for ADULT ZEE-FRAME is JAY.

Related Clinical Trials

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.

Other records listing Equilibrated Bio Systems, 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 7 devices →

Related Devices (Code: JAY)

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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