FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
P.D. METER
K Number: K821083
·
Decision Jun 14, 1982
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
1
Applicant Total
13
Review Days
56
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Basic Information
- Device Name
- P.D. METER
- K Number
- K821083
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.1700
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Medical Equipment Designs, Inc.
- Date Received
- April 19, 1982
- Decision Date
- June 14, 1982
- Product Code
- HLH
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- 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 |
|---|---|---|---|
| HLH | Pupillometer, Manual | FDA class 1 | Ophthalmic |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (HLH), ordered by most recent decision date.
View allOther Clearances by Medical Equipment Designs, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K911308 | CARDIOTRACE-I TRANSTELEPHONIC ECG RECEIV CONSOLE | Sep 11, 1991 | Substantially Equivalent |
| K894152 | MEDITHERM | Jun 11, 1990 | Substantially Equivalent |
| K895375 | MULTISPIRO | Nov 27, 1989 | Substantially Equivalent |
| K851277 | MICROSPIRO-SDS | Apr 19, 1985 | Substantially Equivalent |
| K840908 | CHESTAC-25F SPIROMETER | May 14, 1984 | Substantially Equivalent |
| K840929 | FRC 85 SERIES SPIROMETER | May 14, 1984 | Substantially Equivalent |
| K821081 | CHART PROJECTOR | Jun 14, 1982 | Substantially Equivalent |
| K821084 | UNIVERSAL TRIAL FRAMEE | Jun 14, 1982 | Substantially Equivalent |
| K821107 | EXOPHTHALMOMETER | Jun 14, 1982 | Substantially Equivalent |
| K821082 | TRIAL LENS SET | Jun 14, 1982 | Substantially Equivalent |