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FDA 510(k)

SUTURE REMOVAL TRAY

K-Number: K820423 · 1982-03-10

ApplicantMegaplast, Inc.
Decision Date1982-03-10
Product CodeKDD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUTURE REMOVAL TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Megaplast, Inc.. It received FDA 510(k) clearance on 1982-03-10 under 510(k) number K820423. The device is classified under product code KDD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTURE REMOVAL TRAY?

SUTURE REMOVAL TRAY is a medical device that received FDA 510(k) clearance on 1982-03-10. The listed applicant is Megaplast, Inc.. The 510(k) number is K820423.

When did SUTURE REMOVAL TRAY receive FDA 510(k) clearance?

SUTURE REMOVAL TRAY received FDA 510(k) clearance on 1982-03-10, under 510(k) number K820423.

Who is the listed applicant for SUTURE REMOVAL TRAY?

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

What is the FDA product code for SUTURE REMOVAL TRAY?

The FDA product code for SUTURE REMOVAL TRAY is KDD.

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Other records listing Megaplast, 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.

K822158OPEN HEART TRAY (CUSTOM DESIGNED)K821313SURGICAL UTILITY DRAPEK820136URINARY DRAINAGE BAGK810249TRAY, CATHERIZATION, URETHRALK810250TRAY, IRRIGATIONK810251SYRINGE, ENT

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Related Devices (Code: KDD)

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.

K072814CONVENIENCE KIT FOR SINGLE-INCISION LAPAROSCOPIC SURGERY AND OTHER ADVANCED LAPAROSCOPIC PROCEDURESCovidienK011514INSTRUMENTS FOR ONE TIME USE - DISPOSABLEKencap , Ltd.K971317NATIONAL MEDICAL HEALTHCARE CUSTOM ORTHOPEDIC KITS AND TRAYSNational Healthcare Mfg. Corp.K960456DENVER PARACENTESIS NEEDLE(60-1200) DENVER PARACENTESIS NEEDLE WITH DRAINAGE LINE(60-1100) DENVER PARACENTESIS TRAYDenver Biomaterials, Inc.K936255CUSTOM CV PACKAssociated MedicalK932219SUTURE SET OR LACERATION TRAYS (PACKS)Associated Medical Products Co.

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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