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FDA 510(k)

CANNULA'S CAT #'S 6636, 6624, 6625

K-Number: K791982 · 1979-10-04

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

Device Summary

CANNULA'S CAT #'S 6636, 6624, 6625 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 K791982. The device is classified under product code HMX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNULA'S CAT #'S 6636, 6624, 6625?

CANNULA'S CAT #'S 6636, 6624, 6625 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 K791982.

When did CANNULA'S CAT #'S 6636, 6624, 6625 receive FDA 510(k) clearance?

CANNULA'S CAT #'S 6636, 6624, 6625 received FDA 510(k) clearance on 1979-10-04, under 510(k) number K791982.

Who is the listed applicant for CANNULA'S CAT #'S 6636, 6624, 6625?

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 CANNULA'S CAT #'S 6636, 6624, 6625?

The FDA product code for CANNULA'S CAT #'S 6636, 6624, 6625 is HMX.

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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: HMX)

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.

K010305WEISS RETINAL CANNULAMicron Surgical, Inc.K000457VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIESRetinalabs.ComK970873ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.)American Medical Devices, Inc.K943932STERISEAL OPHTHALMIC CANNULAPharma-Plast, Ltd.K942403INFUSION CANNULAMicrosurgical Technology, Inc.K934844INTER TIP TMicrosurgical Technology, 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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