510(k) K904878
- Device
- SENSI RADS LEAD LATEX RADIATION PROT. GLOVE, STER.
- Applicant
- HPI, INC.
- 510(k) number
- K904878
- Product code
- IWP
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1991-03-07
- Date received
- 1990-10-30
- Regulation
- 892.6500
- Classification name
- Radiographic Protective Glove
- Medical specialty
- Radiology
- Review panel
- Radiology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- JUDITH A GENZALE
- Address
- 825 Beacon St. Suite 11 Newton Centre MA US 02159 02159
FDA Registration Numbers#
- 1063300
- 8043736
- 3006210673
- 3015821396
- 3020118
- 3027157200
- 3013856565
- 3016704566
- 1225473
- 3043648115
- 3008808560
- 3008266585
- 3015391081
- 3010966951
- 9681260
- 3010187802
- 3002532594
- 3017041963
- 2024351
- 3021282544
- 3011344631
- 8041005
- 3012436532
- 3004859241
- 2431224
- 2529126
- 3012314549
- 3016195105
- 3016159368
- 3001970230
- 3018299689
- 3027976674
- 3011209798
- 3008485841
- 3023812384
- 3013632692
- 1828132
- 1319660
- 1000121056
- 3014437893
- 3010273872
- 1222742
- 3008062466
- 3008386507
- 3027157158
- 3030017177
- 3009222501
- 3010220595
- 3012309743
- 3002806603
- 3027815
- 3013522894
- 3006897996
- 2124215
- 3015745029
- 3017299525
- 3015378469
- 3040389667
- 3005972890
- 3008252486
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code IWP #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K920538 | PROTECTIVE RADIOGRAFIC GLOVE | Burkhart Roentgen Intl., Inc. | 1992-05-29 |
| K905086 | HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES | Hpi, Inc. | 1990-12-03 |
| K900972 | RADIATION PROTECTION GLOVES | Infab Corp. | 1990-05-01 |
| K844683 | IMAGEN CHLAMYDIA TEST | Boots-Celltech Diagnostics, Inc. | 1985-02-06 |
Legacy Summary#
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FDA Review#
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