FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CONSIOUS SEDATION (ANALOR P-76)
K Number: K760017
·
Decision Jul 20, 1976
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
53
Applicant Total
5
Review Days
39
Basic Information
- Device Name
- CONSIOUS SEDATION (ANALOR P-76)
- K Number
- K760017
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5330
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- MCKESSON CORP.
- Date Received
- June 11, 1976
- Decision Date
- July 20, 1976
- Product Code
- BZR
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| BZR | Mixer, Breathing Gases, Anesthesia Inhalation | FDA class 2 | Anesthesiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (BZR), ordered by most recent decision date.
Midas Flowmeter; eAVS
FDA 510(k)
FDA Class 2
·Anesthesiology
Maxtec MaxBlend2+p
FDA 510(k)
FDA Class 2
·Anesthesiology
FlowStar Analog Mixer Flowmeter
FDA 510(k)
FDA Class 2
·Anesthesiology
FlowStar Touch Digital Mixer Flowmeter
FDA 510(k)
FDA Class 2
·Anesthesiology
Quality Mix Blender, Oxymixer
FDA 510(k)
FDA Class 2
·Anesthesiology
Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50
FDA 510(k)
FDA Class 2
·Anesthesiology
Other Clearances by MCKESSON CORP.
| K Number | Device Name | ||
|---|---|---|---|
| K771175 | RESUSCITATOR, MS30 | Aug 2, 1977 | Substantially Equivalent |
| K761196 | NITROUS OXIDE SCAVENGING MASK | Dec 13, 1976 | Substantially Equivalent |
| K761195 | ESOPHAGEAL OBTURATION AIRWAY | Dec 9, 1976 | Substantially Equivalent |
| K761194 | HLR QUICK-FIT HEART-LUNG RESUSCITATOR | Dec 9, 1976 | Substantially Equivalent |