EYE TRAY— 510(k) K970722

Substantially Equivalent

Trinity Laboratories, Inc.

FDA 510(k) clearance K970722 for EYE TRAY, Substantially Equivalent on 1997-03-31. Applicant: Trinity Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Trinity Laboratories, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1997-02-27
Decision date: 1997-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salisbury, MD, US

Download summary PDF View on FDA.gov ↗

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More clearances from Trinity Laboratories, Inc.

K981441 — HEART CATH TRAY, STERILE, DISPOSABLE1998-07-10
K974238 — DENTAL TRAY, STERILE, DISPOSABLE1998-02-04
K974286 — CIRCUMCISION TRAY, CAT. NO. 703401997-12-12
K972160 — CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE AGGLUTNATION LATEX TEST1997-08-01
K965201 — O.R. SCRUB PREP TRAY, STERILE, DISPOSABLE1997-02-14

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