FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD

K Number: K844761 · Decision Dec 24, 1984
Classifications
1
FEI Numbers
712
Registration Numbers
712
Same Product Code
54
Applicant Total
22
Review Days
17

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SCHWARTZ/NORRIS CORNEAL LIGHT SHIELD
K Number
K844761
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4750
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Medical Instrument Development Laboratories, Inc.
Date Received
December 7, 1984
Decision Date
December 24, 1984
Product Code
HOY
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
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HOY), ordered by most recent decision date.

View all

Other Clearances by Medical Instrument Development Laboratories, Inc.

K Number Device Name
K102222 ULTIMATE VIT ENHAMCER (UVE)
K020911 MID LABS AUTONOMOUS VIT ENHANCER (AVE)
K992943 VIT ENHANCER
K971067 DIGI-INJECTOR
K950287 UNIVIT PROBE
K934600 MICRODRIVE
K932669 SUPRA-VIT(TM)
K932131 MID LABS TWIN ILLUMINATOR
K924222 MID LABS, INC. VIT MATE
K851610 COMBINED MVS SYSTEMS
Search all 22 clearances from Medical Instrument Development Laboratories, Inc. →