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FDA 510(k)

LAPAROMED LIGATING LOOP

K-Number: K921053 · 1992-08-06

ApplicantLaparomed Corp.
Decision Date1992-08-06
Product CodeKCJ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LAPAROMED LIGATING LOOP is the device name listed in this FDA 510(k) record. The listed applicant is Laparomed Corp.. It received FDA 510(k) clearance on 1992-08-06 under 510(k) number K921053. The device is classified under product code KCJ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPAROMED LIGATING LOOP?

LAPAROMED LIGATING LOOP is a medical device that received FDA 510(k) clearance on 1992-08-06. The listed applicant is Laparomed Corp.. The 510(k) number is K921053.

When did LAPAROMED LIGATING LOOP receive FDA 510(k) clearance?

LAPAROMED LIGATING LOOP received FDA 510(k) clearance on 1992-08-06, under 510(k) number K921053.

Who is the listed applicant for LAPAROMED LIGATING LOOP?

The FDA 510(k) record lists Laparomed Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROMED LIGATING LOOP?

The FDA product code for LAPAROMED LIGATING LOOP is KCJ.

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Other records listing Laparomed Corp. 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.

K934527FASCIA STITCHERK930569LAPAROMED LAPAROSCOPIC RETRACTOR SYSTEMK921921CATHETER CHOLANGIOGRAPHYK921006LAPAROSCOPIC RETRACTOR SYSTEMK914066ELECTROSURGICAL CUTTING/COAGULATION DEVICE/ACCESSK910074LAPAROMED HOOK/SPATULA DEVICE

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Related Devices (Code: KCJ)

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.

K923679ENDOPATH TISSUE RETAINING COMPONENTEthicon Endo-Surgery, Inc.K894369APDYNE PHENOL APPLICATOR KITApdyne Medical Co.K832667LUCAE'S EAR & NASAL APPLICATORSKells Medical, 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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