Atlas FDA

STETSKINS

FDA 510(k) clearance K930118 · decided 1993-03-26

Clearance details

K-number
K930118
Device name
STETSKINS
Applicant
Nova Diversified Concepts
Decision
Substantially Equivalent
Date received
1993-01-11
Decision date
1993-03-26
Days to decision
74 days
Clearance type
Traditional
Product code
BZS
Device class
1
Regulation number
868.1930
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Columbus, OH, 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
DISPOSABLE STETHOSCOPE HEAD COVER (K935146)Modern Medical Devices, Inc.1994-07-11
SUPRA SCOPE (K801050)Warner-Lambert Co.1980-05-14

Recalls involving this device

No recalls on record reference this clearance.