510(k) K922576
- Device
- Aesculap Manual Endoscopic Instruments
- Applicant
- AESCULAP, INC.
- 510(k) number
- K922576
- Product code
- GEI
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1993-06-10
- Date received
- 1992-06-01
- Regulation
- 878.4400
- Classification name
- Electrosurgical, Cutting & Coagulation & Accessories
- Medical specialty
- General, Plastic Surgery
- Review panel
- General, Plastic Surgery
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Statement
- Third party reviewed
- N
- Source
- FDA openFDA 510(k) dataset plus migrated FDA.report data
Related Records
Applicant Contact
- Contact
- VICTORIA MACKINNON
- Address
- 1000 Gateway Blvd. South San Francisco CA US 94080 94080
FDA Registration Numbers
- 3002808148
- 1450662
- 3005677568
- 3038715747
- 3010288205
- 3010402752
- 3016087306
- 3013820501
- 3026612481
- 3030926959
- 3007593944
- 3013917867
- 3030495752
- 3010377594
- 3008720584
- 3015515531
- 3011277660
- 8040537
- 9614969
- 3004464325
- 9617429
- 1421101
- 3008933393
- 3007047889
- 3015453963
- 2183744
- 3013188547
- 3012757453
- 3030230686
- 3007007790
- 3012259264
- 3008805497
- 3014939461
- 3020142587
- 1216677
- 9612074
- 2938071
- 1651252
- 3009241989
- 1313525
- 3009822485
- 2649614
- 2031093
- 3030447506
- 1643264
- 3011050570
- 3007353760
- 1051614
- 3013376016
- 1319660
- 2085947
- 1423537
- 1718850
- 3008843439
- 3010305275
- 3033589330
- 3006950086
- 8043398
- 3003678543
- 2028523
- 3027339877
- 8010877
- 8010890
- 1064858
- 3017210488
- 2126666
- 3002807314
- 3007675948
- 3010687973
- 2916714
- 3009756327
- 3011120183
- 8010177
- 3007113251
- 2424366
- 3030733800
- 3007305485
- 3004904811
- 3004530184
Source Documents
FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON
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