Atlas FDA

DOUBLE & SINGLE TANTALUM CLIPS

FDA 510(k) clearance K840207 · decided 1984-03-29

Clearance details

K-number
K840207
Device name
DOUBLE & SINGLE TANTALUM CLIPS
Applicant
Storz Instrument Co.
Decision
Substantially Equivalent
Date received
1984-01-19
Decision date
1984-03-29
Days to decision
70 days
Clearance type
Traditional
Product code
HQW
Device class
2
Regulation number
886.3100
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Mchenry, IL, 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
GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP (K897119)Grieshaber & Co.1990-04-12
RETINAL TAAK (K901275)Alcon Surgical, Inc.1990-03-23

Recalls involving this device

No recalls on record reference this clearance.