Calipers, Mcgaw Skinfold
FDA 510(k) K760520 · Mcgaw Laboratories
510(k) numberK760520
Submission
- Device name
- Calipers, Mcgaw Skinfold
- Applicant
- Mcgaw Laboratories
Mchenry, IL, US - Received
- August 26, 1976
- Decision date
- November 12, 1976
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- BXW – Calibrator, Volume, Gas
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.1870
- Specialty
- Anesthesiology
Other 510(k)s with product code BXW
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K853848 | Respiratory Diagnostic Equipment CalibratorBXW · Traditional | Medical Graphics Corp. | 12/05/1985SE |
| K831758 | Flow-Calibration ModuleBXW · Traditional | The Perkin-Elmer Corp. | 07/19/1983SE |
| K830898 | Syringe 500BC Be #7000BXW · Traditional | Instrumentation Industries, Inc. | 05/16/1983SE |
| K812765 | Datascribe #DS-40BXW · Traditional | Timeter Instrument Corp. | 11/16/1981SE |
| K810290 | Ohio Cal-ChekBXW · Traditional | Ohio Medical Products | 02/12/1981SE |
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Questions and answers
When was Calipers, Mcgaw Skinfold cleared by the FDA?
Calipers, Mcgaw Skinfold (K760520) received a 510(k) decision of Substantially Equivalent on November 12, 1976, 78 days after the submission was received.
What is the product code of K760520?
The FDA product code is BXW – Calibrator, Volume, Gas, a Class I (low risk) device regulated under 21 CFR 868.1870.