FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OPHTHALAS DYE OPHTHALMIC LASER

K Number: K873460 · Decision Oct 29, 1987
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
11
Review Days
62

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Basic Information

Device Name
OPHTHALAS DYE OPHTHALMIC LASER
K Number
K873460
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4390
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Biophysic Medical, Inc.
Date Received
August 28, 1987
Decision Date
October 29, 1987
Product Code
HQF
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
HQF Laser, Ophthalmic

Similar 510(k) Clearances

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Other Clearances by Biophysic Medical, Inc.

K Number Device Name
K953399 NEEDLE OR CUTTER
K893035 OPHTHASCAN 'S' MINI-A
K890509 INDIRECT OPHTHALMOSCOPE ACCESSORY DELIVERY SYSTEM
K884595 OPHTHASCAN MINI-B
K884456 STERILE DISPOSABLE ENDOCULAR PROBE
K883719 INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM
K881494 FOUR MODIFICATIONS TO OPHTHALAS ARGON/DYE LASER
K881459 NANOLAS ND:YAG OPHTHALMIC LASER
K853116 PAXIAL
K844686 OPHTHASCAN B
Search all 11 clearances from Biophysic Medical, Inc. →