510(k) K760521
- Device
- TAPE MEASURE
- Applicant
- MCGAW LABORATORIES
- 510(k) number
- K760521
- Product code
- KTZ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1976-11-12
- Date received
- 1976-08-26
- Regulation
- 888.4150
- Classification name
- Caliper
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 4221 Richmond Rd., NW Walker MI US 49534 49534
FDA Registration Numbers#
- 9614069
- 3022862651
- 3008812560
- 3009165919
- 3015876273
- 3006215390
- 3036756245
- 8040233
- 3005325790
- 1834379
- 3034676720
- 3003334541
- 3016965929
- 3004142400
- 3015212339
- 3010531060
- 3003418325
- 1720747
- 9610612
- 3006059835
- 3013552516
- 3007773213
- 3008770252
- 3019878714
- 3008572101
- 1066741
- 3003956316
- 3016050940
- 3001297506
- 3003597504
- 1417592
- 3009106092
- 1043534
- 3010536692
- 3005739886
- 9611274
- 3005031160
- 9613079
- 1032347
- 1222742
- 1646747
- 3012447612
- 8040278
- 1219518
- 9680515
- 2183301
- 3006395932
- 3010197239
- 3010370500
- 3004464325
- 3015207155
- 9611367
- 3005823819
- 9680002
- 3044819802
- 3005641619
- 3009888740
- 1828464
- 3000270450
- 3015542154
- 3013055499
- 3004598675
- 3013846070
- 3004371426
- 9610621
- 3009513193
- 1224360
- 9614093
- 3011513267
- 3005061536
- 2249529
- 1818910
- 3005273623
- 3038718579
- 3033509898
- 3005528784
- 3003882387
- 3003120897
- 3010455030
- 3021666757
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code KTZ #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K921266 | NK MEDICAL MICROMETER, MODEL MC001 | Nk Biotechnical Engineering Co. | 1992-07-14 |
| K841687 | SKYNDEX ELECTRONIC BODY FAT CALCULA | Caldwell, Justiss & Co., Inc. | 1984-06-28 |
| K831898 | SCOLIMETER | Dr. Micheal A. Sabia | 1983-07-19 |
| K820659 | A CALIPER | Twin City Surgical, Inc. | 1982-03-19 |
| K810116 | ISOROBIC SKINFOLD CALIPER | Fitness Motivation Institute of America | 1981-02-04 |
| K800363 | PARKE-DAVIS TOTAL KNEE PROSTHESIS | Warner-Lambert Co. | 1980-03-10 |
Legacy Summary#
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FDA Review#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases