Browse hierarchy: [General, Plastic Surgery (SU)](/submissions/SU) → [Subpart F — Therapeutic Devices](/submissions/SU/subpart-f%E2%80%94therapeutic-devices) → [21 CFR 878.5070](/submissions/SU/subpart-f%E2%80%94therapeutic-devices/878.5070) → FZH — Apparatus, Air Handling, Room

# FZH · Apparatus, Air Handling, Room

_General, Plastic Surgery · 21 CFR 878.5070 · Class 2_

**Canonical URL:** https://fda.innolitics.com/submissions/SU/subpart-f%E2%80%94therapeutic-devices/FZH

## Overview

- **Product Code:** FZH
- **Device Name:** Apparatus, Air Handling, Room
- **Regulation:** [21 CFR 878.5070](/submissions/SU/subpart-f%E2%80%94therapeutic-devices/878.5070)
- **Device Class:** 2
- **Review Panel:** [General, Plastic Surgery](/submissions/SU)

## Identification

Air-handling apparatus for a surgical operating room is a device intended to produce a directed, nonturbulent flow of air that has been filtered to remove particulate matter and microorganisms to provide an area free of contaminants to reduce the possibility of infection in the patient.

## Classification Rationale

Class II (special controls). The device, when it is an air handling bench apparatus, an air handling room apparatus, or an air handling enclosure apparatus, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 878.9.

## Special Controls

*Classification.* Class II (special controls). The device, when it is an air handling bench apparatus, an air handling room apparatus, or an air handling enclosure apparatus, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 878.9.

## Recent Cleared Devices (4 of 4)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [K923233](https://fda.innolitics.com/submissions/SU/subpart-f%E2%80%94therapeutic-devices/FZH/K923233.md) | CARDIO-PAK LAPAROTOMY PACK | Cardio-Med-Associates, Inc. | Mar 20, 1993 | SESK |
| [K875305](https://fda.innolitics.com/submissions/SU/subpart-f%E2%80%94therapeutic-devices/FZH/K875305.md) | MODEL UCA / SPEC SYSTEM UCA | Spec Systems, Inc. | Jan 27, 1988 | SESE |
| [K871901](https://fda.innolitics.com/submissions/SU/subpart-f%E2%80%94therapeutic-devices/FZH/K871901.md) | ULTRAFLOW | Custom Industries, Inc. | Jun 1, 1987 | SESE |
| [K770084](https://fda.innolitics.com/submissions/SU/subpart-f%E2%80%94therapeutic-devices/FZH/K770084.md) | OPERATING ROOM VENTILATOR | Dupaco, Inc. | Feb 23, 1977 | SESE |

## Top Applicants

- Cardio-Med-Associates, Inc. — 1 clearance
- Custom Industries, Inc. — 1 clearance
- Dupaco, Inc. — 1 clearance
- Spec Systems, Inc. — 1 clearance

---

**Source:** [https://fda.innolitics.com/submissions/SU/subpart-f%E2%80%94therapeutic-devices/FZH](https://fda.innolitics.com/submissions/SU/subpart-f%E2%80%94therapeutic-devices/FZH)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com
