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FDA 510(k)

PARAPLAST EXTRA TISSUE EMBEDDING MED.

K-Number: K842053 · 1984-06-26

ApplicantSherwood Medical Co.
Decision Date1984-06-26
Product CodeKEO
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

PARAPLAST EXTRA TISSUE EMBEDDING MED. is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1984-06-26 under 510(k) number K842053. The device is classified under product code KEO. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARAPLAST EXTRA TISSUE EMBEDDING MED.?

PARAPLAST EXTRA TISSUE EMBEDDING MED. is a medical device that received FDA 510(k) clearance on 1984-06-26. The listed applicant is Sherwood Medical Co.. The 510(k) number is K842053.

When did PARAPLAST EXTRA TISSUE EMBEDDING MED. receive FDA 510(k) clearance?

PARAPLAST EXTRA TISSUE EMBEDDING MED. received FDA 510(k) clearance on 1984-06-26, under 510(k) number K842053.

Who is the listed applicant for PARAPLAST EXTRA TISSUE EMBEDDING MED.?

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

What is the FDA product code for PARAPLAST EXTRA TISSUE EMBEDDING MED.?

The FDA product code for PARAPLAST EXTRA TISSUE EMBEDDING MED. is KEO.

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Other records listing Sherwood Medical Co. 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.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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Related Devices (Code: KEO)

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.

K893772TISSUE EMBEDDING MEDIUMStephens ScientificK862223MICRO THIN* PARAFFINRichard-Allan Medical Ind., Inc.K862141HISTOLOGY PARAFFINErie Scientific Co.K861270BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.Surgipath Medical Industries, Inc.K833071TECHNICON PARACUTTechnicon Instruments Corp.K831580PARAFFIN INFILTRATION MEDIUMSurgipath Medical Industries, 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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