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Pinpoint

FDA UDI

Class II (US FDA UDI)

by Novadaq Technologies Inc

Identity

Trade Name
PINPOINT FDA UDI
Generic Name
Endoscope video camera FDA UDI
Device Name
Camera FDA UDI
Model / Reference
PC9002 FDA UDI
Description
Camera FDA UDI

Identifiers

Catalog Number
PC9002 FDA UDI
Primary DI / UDI-DI
00858701006551 FDA UDI
510(k) Number
K150956 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscope video camera FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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
Sterilization Method
Hydrogen Peroxide FDA UDI

Category: Endoscope video camera

Pinpoint by Novadaq Technologies Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope video camera.

Cleared under the same submission

K150956 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novadaq Technologies Inc

Sources (1)

  • FDA UDI c3ce47ab-f7d3-44cf-a0f0-338b5ca01bb9 36 fields · synced Jun 1, 2026