Sechrist Industries, Inc.

FDA UDI

Class II (US FDA UDI)

by Sechrist Industries Inc

Identity

Trade Name: Sechrist Industries, Inc. FDA UDI
Generic Name: Hyperbaric chamber, stationary FDA UDI
Device Name: HBO CHMBER,36IN,ELECT CNTRL,ENGLISH,BLUE FDA UDI
Model / Reference: 3600E-00 FDA UDI
Description: HBO CHMBER,36IN,ELECT CNTRL,ENGLISH,BLUE FDA UDI

Identifiers

Primary DI / UDI-DI: 00852682007934 FDA UDI
510(k) Number: K052713 FDA UDI
FDA Product Code: CBF FDA UDI
GMDN Term: Hyperbaric chamber, stationary FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5470 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Width — 53 Inch FDA UDI
Height — 81 Inch FDA UDI
Weight — 2220 Pound FDA UDI
Depth — 112 Inch FDA UDI

Category: Hyperbaric chamber, stationary

Sechrist Industries, Inc. by Sechrist Industries Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K052713 also covers:

Sechrist Industries, Inc. — Sechrist Industries Inc

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Sechrist Industries Inc

Sources (1)

FDA UDI 2d193668-24e0-40f8-ad8c-ec0684a6691b 36 fields · synced May 30, 2026