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Instavac C

FDA UDI

Class II (US FDA UDI)

by Ohio Medical LLC

Identity

Trade Name
Instavac C FDA UDI
Generic Name
General-purpose surgical suction system, electric FDA UDI
Device Name
Portable Suction Pump FDA UDI
Model / Reference
Instavac C FDA UDI
Description
Portable Suction Pump FDA UDI

Identifiers

Primary DI / UDI-DI
00628101609498 FDA UDI
510(k) Number
K933902 FDA UDI
FDA Product Code
BTA FDA UDI
GMDN Term
General-purpose surgical suction system, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose surgical suction system, electric

Instavac C by Ohio Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose surgical suction system, electric.

Cleared under the same submission

K933902 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ohio Medical LLC

Sources (1)

  • FDA UDI 5f231139-aa26-426f-8e1c-f1d43fdf67f2 35 fields · synced May 30, 2026