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FDA 510(k)

CEMENT-PICK

K-Number: K822108 · 1982-08-11

ApplicantBio-Blitz, Inc.
Decision Date1982-08-11
Product CodeGAF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CEMENT-PICK is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Blitz, Inc.. It received FDA 510(k) clearance on 1982-08-11 under 510(k) number K822108. The device is classified under product code GAF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEMENT-PICK?

CEMENT-PICK is a medical device that received FDA 510(k) clearance on 1982-08-11. The listed applicant is Bio-Blitz, Inc.. The 510(k) number is K822108.

When did CEMENT-PICK receive FDA 510(k) clearance?

CEMENT-PICK received FDA 510(k) clearance on 1982-08-11, under 510(k) number K822108.

Who is the listed applicant for CEMENT-PICK?

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

What is the FDA product code for CEMENT-PICK?

The FDA product code for CEMENT-PICK is GAF.

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.

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Other records listing Bio-Blitz, 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.

K822109SHOVEL RETRACTOR

Related Devices (Code: GAF)

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.

K023688LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPERLeMaitre Vascular, Inc.K935357SNAP RECIPROCATING SAWSurgiquip, Inc.K890374ABDOMINAL SPATULAKinetic Medical ProductsK882793PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINEPmt Corp.

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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