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FDA 510(k)

PREPACELL-STERILE-BONE MARROW ASPIR

K-Number: K833438 · 1984-02-09

ApplicantApplied Medical Devices, Inc.
Decision Date1984-02-09
Product CodeKDD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PREPACELL-STERILE-BONE MARROW ASPIR is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Devices, Inc.. It received FDA 510(k) clearance on 1984-02-09 under 510(k) number K833438. 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 PREPACELL-STERILE-BONE MARROW ASPIR?

PREPACELL-STERILE-BONE MARROW ASPIR is a medical device that received FDA 510(k) clearance on 1984-02-09. The listed applicant is Applied Medical Devices, Inc.. The 510(k) number is K833438.

When did PREPACELL-STERILE-BONE MARROW ASPIR receive FDA 510(k) clearance?

PREPACELL-STERILE-BONE MARROW ASPIR received FDA 510(k) clearance on 1984-02-09, under 510(k) number K833438.

Who is the listed applicant for PREPACELL-STERILE-BONE MARROW ASPIR?

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

What is the FDA product code for PREPACELL-STERILE-BONE MARROW ASPIR?

The FDA product code for PREPACELL-STERILE-BONE MARROW ASPIR is KDD.

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Other records listing Applied Medical Devices, 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.

K843885PERCUTANEOUS ASPIRATION BIOPSY TRAYK843883STERILE PERCUTANEOUS TRANSHEPATIC CHOLANK843884GENERAL UTILITY TRAY SYSTEMK840904ACCU-CULT FECAL OCCULT BLOOD TESTK842591ULTRASOUND PROBE COVERS-STERILEK833720TRANSTHORACIC/TRANSABDOMINAL-TRAY

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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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