SCISSORS, IRIS— 510(k) K770019

Substantially Equivalent

J. Sklar Mfg. Co., Inc.

FDA 510(k) clearance K770019 for SCISSORS, IRIS, Substantially Equivalent on 1977-01-12. Applicant: J. Sklar Mfg. Co., Inc.. Device class: 1.

Clearance details

Applicant: J. Sklar Mfg. Co., Inc.
Product code: Code HNF
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1977-01-05
Decision date: 1977-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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K842111 — KOGAN ENDOSPECULUM 9-1/21984-06-19
K822448 — SCISSORS, VARIOUS1982-09-14
K802457 — KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-66101981-01-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.