Atlas FDA

OPTHA PREP

FDA 510(k) clearance K871706 · decided 1987-05-18

Clearance details

K-number
K871706
Device name
OPTHA PREP
Applicant
Treace Medical, Inc.
Decision
Substantially Equivalent
Date received
1987-05-01
Decision date
1987-05-18
Days to decision
17 days
Clearance type
Traditional
Product code
HMT
Device class
2
Regulation number
878.4370
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Memphis, TN, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPE (K945738)Visitec Co.1995-02-14
STERILE DISPOSABLE DRAPE/OPHTHALMIC SURGERY (K905460)Angiosystems, Inc.1991-02-06
SOLOS EYESITE DRAPES (K872620)Solos Ophthalmology1987-07-31
SURGICAL DRAPES, OPHTHALMIN (K854613)Charles Atkins & Co.1986-02-13
DRAIN-R-DRAPE(EYE (K831340)Sur-Tech, Inc.1983-06-08
EYE DRAPE (K830822)CooperVision, Inc.1983-04-06

Recalls involving this device

No recalls on record reference this clearance.