FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
GENESIS INSUFFLATING CATHETER
K Number: K903669
·
Decision Sep 12, 1990
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
115
Applicant Total
15
Review Days
30
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Basic Information
- Device Name
- GENESIS INSUFFLATING CATHETER
- K Number
- K903669
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.6810
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- General Medical Co.
- Date Received
- August 13, 1990
- Decision Date
- September 12, 1990
- Product Code
- BSY
- 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 |
|---|---|---|---|
| BSY | Catheters, Suction, Tracheobronchial | FDA class 1 | Anesthesiology |
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Other Clearances by General Medical Co.
| K Number | Device Name | ||
|---|---|---|---|
| K926269 | PROCEDURE KIT | Aug 27, 1993 | Unknown |
| K912975 | OPERAND LUBRICATING JELLY | Sep 27, 1991 | Substantially Equivalent |
| K912132 | OPERAND LUBRICATING JELLY | Aug 7, 1991 | Substantially Equivalent |
| K900110 | OPERAND* LUBRICATING JELLY | May 2, 1990 | Substantially Equivalent |
| K853635 | SUBDERM TM | Dec 20, 1985 | Substantially Equivalent |
| K844652 | C.A.S.E. CONTAINER | Dec 12, 1984 | Substantially Equivalent |
| K831320 | DRIONIC | Jul 19, 1983 | Substantially Equivalent |
| K820689 | C.S.R. WRAPPERS | Apr 9, 1982 | Substantially Equivalent |
| K820521 | STERILIZATION WRAP | Mar 18, 1982 | Substantially Equivalent |
| K802231 | AIR VIVA II | Oct 10, 1980 | Substantially Equivalent |