Atlas FDA

HOOK, IRIS, SHEPARD U-SHAPED

FDA 510(k) clearance K770103 · decided 1977-01-25

Clearance details

K-number
K770103
Device name
HOOK, IRIS, SHEPARD U-SHAPED
Applicant
Edward Weck, Inc.
Decision
Substantially Equivalent
Date received
1977-01-17
Decision date
1977-01-25
Days to decision
8 days
Clearance type
Traditional
Product code
HNQ
Device class
1
Regulation number
886.4350
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
OPHTEC ENCLAVATION NEEDLE (K030471)Ophtec, USA2003-04-17
STEPHENS DISPOSABLE HOOKS (K022842)Stephens Instruments2002-11-01
PRISMA DISPOSABLE IRRIGATING IRIS HOOK (K874991)Advanced Surgical Products, Inc.1988-04-13
LOOK LENS LOOPS (K870440)Look, Inc.1987-02-20
DISPOSAL SURGICAL INSTRUMENTS FOR OPHTHALMOLOGY (K864292)Eye-Ko, Inc.1986-12-29
THORTON TITANIUM HOOK ANGLED RIGHT (K863988)Keeler Instruments, Inc.1986-10-31
BONN MICRO IRIS HOOK (NON-STERILE) #7613 (K801469)Edward Weck, Inc.1980-07-28
HOOKS #'S 7600,7602,7603,7616 (K791985)Edward Weck, Inc.1979-10-04
HOOK, IRIS, HERSHMAN (K770098)Edward Weck, Inc.1977-01-24

Recalls involving this device

No recalls on record reference this clearance.