DRILL, DENTAL— 510(k) K801887

Substantially Equivalent

Aesculap Instruments Corp.

FDA 510(k) clearance K801887 for DRILL, DENTAL, Substantially Equivalent on 1980-08-20. Applicant: Aesculap Instruments Corp.. Device class: 1.

Clearance details

Applicant: Aesculap Instruments Corp.
Product code: Code DZA
Device class: Class 1
Regulation: 21 CFR 872.4130
Advisory panel: Dental
Date received: 1980-07-28
Decision date: 1980-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DZA

K984508 — SURGICAL CONTRA-ANGLE HANDPIECES, MODELS 975 AE,979 E/KM, 985 AE, 986 AE, 988 E/KM AND SURGICAL STRAIGHT HANDPIECES MOD1999-06-25
K962979 — S-53 INTRORAL DENTAL SYSTEM1996-09-25
K954790 — PROFILE NICKEL TITANIUM ROTARY INSTRUMENTS1996-01-16
K914724 — ADA SHANK EXTENSION1993-07-27
K905418 — GATES GLIDDEN DRILLS1991-07-25

More clearances from Aesculap Instruments Corp.

K885046 — INSITUCAT VALVE STRIPPER1990-02-28
K890182 — PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV1990-02-28
K890443 — CASPAR SCALP CLIP, APPLIER1989-06-15
K893121 — ROBOTRAC (TM) RETRACTOR ARM1989-06-01
K884057 — ELAN-E DISPOSABLE DRAPE1988-10-19

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