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FDA 510(k)

RULER, WECK SCOTT

K-Number: K781715 · 1978-12-04

ApplicantEdward Weck, Inc.
Decision Date1978-12-04
Product CodeHOE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RULER, WECK SCOTT 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 1978-12-04 under 510(k) number K781715. The device is classified under product code HOE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RULER, WECK SCOTT?

RULER, WECK SCOTT is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Edward Weck, Inc.. The 510(k) number is K781715.

When did RULER, WECK SCOTT receive FDA 510(k) clearance?

RULER, WECK SCOTT received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781715.

Who is the listed applicant for RULER, WECK SCOTT?

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 RULER, WECK SCOTT?

The FDA product code for RULER, WECK SCOTT is HOE.

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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: HOE)

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.

K881094KOI(TM) BLADE GAUGE, MODEL KOI-132CooperVision, Inc.K813315CALIPER-OPTHALMICDesign Research Assoc., Inc.K820050KREMER BLADE GAUGEAccutome, Inc.K812011BLADE GAUGEKoi, Inc.K801937BLEPHAROMETERAztec Medical Products, Inc.K792383KELMAN DIPSTICKV. Mueller O.V. Baxter Healthcare Corp.

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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