Dr. Fog® Anti-fog Solution
GUDID 20887761000036
Intended to be used as an anti-fog agent for endoscopic camera lenses
ASPEN SURGICAL PRODUCTS, INC.
Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution Endoscopic antifog solution| Primary Device ID | 20887761000036 |
| NIH Device Record Key | 91a9a333-63a7-4e97-8824-c0ced1044255 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Dr. Fog® Anti-fog Solution |
| Version Model Number | DF-3100B |
| Company DUNS | 027680821 |
| Company Name | ASPEN SURGICAL PRODUCTS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887761000032 [Primary] |
| GS1 | 10887761000039 [Package] Contains: 00887761000032 Package: [20 Units] In Commercial Distribution |
| GS1 | 20887761000036 [Package] Contains: 10887761000039 Package: [15 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K932449
FDA Product Code
| OCT | Anti fog solution and accessories, endoscopy |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-12-18 |
| Device Publish Date | 2016-09-17 |
On-Brand Devices [Dr. Fog® Anti-fog Solution]
| 20887761000036 | Intended to be used as an anti-fog agent for endoscopic camera lenses |
| 00840113200603 | Intended to be used as an anti-fog agent for endoscopic camera lenses |
Trademark Results [Dr. Fog]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 DR. FOG 97488676 not registered Live/Pending |
1000097507 ONTARIO INC. 2022-07-05 |
 DR. FOG 88713883 not registered Live/Pending |
Asaro, Christopher 2019-12-03 |
 DR. FOG 86562655 5052318 Live/Registered |
PREMIUM LIQUID LABS INC. 2015-03-12 |
 DR. FOG 74181779 1730491 Live/Registered |
ASPEN SURGICAL PRODUCTS, INC. 1991-07-02 |
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