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FDA 510(k)

ZEE-FRAME

K-Number: K781509 · 1978-09-26

ApplicantEquilibrated Bio Systems, Inc.
Decision Date1978-09-26
Product CodeJAY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

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 1978-09-26 under 510(k) number K781509. 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 ZEE-FRAME?

ZEE-FRAME is a medical device that received FDA 510(k) clearance on 1978-09-26. The listed applicant is Equilibrated Bio Systems, Inc.. The 510(k) number is K781509.

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

ZEE-FRAME received FDA 510(k) clearance on 1978-09-26, under 510(k) number K781509.

Who is the listed applicant for 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 ZEE-FRAME?

The FDA product code for 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.

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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.

K892705EBS2605 INFANT HUGGERK855102MONARK 869 ERGOMETERK843996TURBOAIRE CHALLANGER ENVIRONMENTAL AIR CONTROLLERK791294SPIROCALK790410ADULT ZEE-FRAMEK781386EBS 775 TONOMETER

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.

K944988CUSTOM MEDICAL SUSPENSION STRAPCustom Medical Specialties, Inc.K873491BLOCK, BITE, INTUBATIONB&B Medical Technologies, Inc.K860583DALE HEAD BAND ANESTHESIA CIRCUIT TUBE HOLDER 1315Dale Medical Products, Inc.K850924JEE FRAME (VENTILATOR CIRCUIT SUPPORT)Vulcan Laboratories, Inc.K850309COMFIT PLUS ENDOTRACHEAL TUBE HOLDER & BITE BLOCKAckrad LaboratoriesK840844ENDO-SECUREExidyne, 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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