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FDA 510(k)

SKILCRAFT

K-Number: K880785 · 1988-03-11

ApplicantPennsylvania Association For the Blind
Decision Date1988-03-11
Product CodeKDD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SKILCRAFT is the device name listed in this FDA 510(k) record. The listed applicant is Pennsylvania Association For the Blind. It received FDA 510(k) clearance on 1988-03-11 under 510(k) number K880785. 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 SKILCRAFT?

SKILCRAFT is a medical device that received FDA 510(k) clearance on 1988-03-11. The listed applicant is Pennsylvania Association For the Blind. The 510(k) number is K880785.

When did SKILCRAFT receive FDA 510(k) clearance?

SKILCRAFT received FDA 510(k) clearance on 1988-03-11, under 510(k) number K880785.

Who is the listed applicant for SKILCRAFT?

The FDA 510(k) record lists Pennsylvania Association For the Blind as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SKILCRAFT?

The FDA product code for SKILCRAFT is KDD.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Pennsylvania Association For the Blind 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.

K903486MASK, SURGICAL-DISPOSABLE NSN 6510-00-982-7493

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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