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FDA 510(k)

SPATULA'S #'S 7618,7248,7240,7242,5108

K-Number: K791983 · 1979-10-04

ApplicantEdward Weck, Inc.
Decision Date1979-10-04
Product CodeHND
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPATULA'S #'S 7618,7248,7240,7242,5108 is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1979-10-04 under 510(k) number K791983. The device is classified under product code HND. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPATULA'S #'S 7618,7248,7240,7242,5108?

SPATULA'S #'S 7618,7248,7240,7242,5108 is a medical device that received FDA 510(k) clearance on 1979-10-04. The listed applicant is Edward Weck, Inc.. The 510(k) number is K791983.

When did SPATULA'S #'S 7618,7248,7240,7242,5108 receive FDA 510(k) clearance?

SPATULA'S #'S 7618,7248,7240,7242,5108 received FDA 510(k) clearance on 1979-10-04, under 510(k) number K791983.

Who is the listed applicant for SPATULA'S #'S 7618,7248,7240,7242,5108?

The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPATULA'S #'S 7618,7248,7240,7242,5108?

The FDA product code for SPATULA'S #'S 7618,7248,7240,7242,5108 is HND.

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Other records listing Edward Weck, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K915378WECK TROCARK914690LM15(TM), CATALOG NUMBER - 523821K911915HEMOCLIP IIK914470PNEUMO-SEAL(TM)K911272ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705K902108HEM-O-LOK(TM)

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Related Devices (Code: HND)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K863990THORNTON TITANIUM SILVER SPATULAKeeler Instruments, Inc.K810937ANIS IRRIGATING SPATULAAmerican V. MuellerK801609MADDOX LENS SPATULA CAT. #7245Edward Weck, Inc.K801608MCCULLEY CONTINUOUS SUTURE TIGHTNEREdward Weck, Inc.K761253CYCLODIALYSIS SPAT. 15MM BLADE TITANIUMEdward Weck, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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