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FDA 510(k)

STERI-VAC POWER UNITS

K-Number: K781486 · 1978-09-27

ApplicantCpac, Inc.
Decision Date1978-09-27
Product CodeEHZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STERI-VAC POWER UNITS is the device name listed in this FDA 510(k) record. The listed applicant is Cpac, Inc.. It received FDA 510(k) clearance on 1978-09-27 under 510(k) number K781486. The device is classified under product code EHZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERI-VAC POWER UNITS?

STERI-VAC POWER UNITS is a medical device that received FDA 510(k) clearance on 1978-09-27. The listed applicant is Cpac, Inc.. The 510(k) number is K781486.

When did STERI-VAC POWER UNITS receive FDA 510(k) clearance?

STERI-VAC POWER UNITS received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781486.

Who is the listed applicant for STERI-VAC POWER UNITS?

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

What is the FDA product code for STERI-VAC POWER UNITS?

The FDA product code for STERI-VAC POWER UNITS is EHZ.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cpac, 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.

K110867STERI-DENT, STERI-SUREK094026STERI-DENT, STERI-SUREK771071PORTO-VACK771070DRY HEAT STERILIZER

Related Devices (Code: EHZ)

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.

K973248IMTEC BONE COLLECTOR SYSTEMImtec Corp.K941164TAP EXPRESS EJECTORTap Express, Inc.K911072SUPER EVACRETRACTOR, DISPOSABLE ORAL EVACUATORA & F ProductsK903718OROSCOPE MODEL NUMBER COS-100Cygnus Instruments, Inc.K892881DENTAL SANI-SLEEVE STERILE 60MM X 1650MM #1101Nieusma R & D, Inc.K892882DENTAL SANI-SLEEVE STERILE 100MM X 2200MM #1102Nieusma R & D, 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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